A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
Cultivation Techniques and Medicinal Properties of Pleurotus spp. Andrej Gregori1,2*, Mirjan [vagelj3 and Jure Pohleven4,5
1SRC Bistra Ptuj, Slovenski trg 6, SI-2250 Ptuj, Slovenia
2Institute for Natural Sciences, Ulica bratov U~akar 108, SI-1000 Ljubljana, Slovenia
3Department of Chemical, Biochemical and Ecology Engineering, University of Ljubljana,
4Department of Pharmaceutical Biology, Faculty of Pharmacy, University of Ljubljana,
5Department of Biotechnology, Jo`ef Stefan Institute, Jamova 39, SI-1000 Ljubljana, Slovenia
The genus Pleurotus (oyster mushroom) comprises some the most popular edible mush-
rooms due to their favourable organoleptic and medicinal properties, vigorous growth andundemanding cultivation conditions. It can be cultivated on log and a wide variety ofagroforestry (by-)products, weeds and wastes for the production of food, feed, enzymesand medicinal compounds, or for waste degradation and detoxification. Many differenttechniques and substrates have been successfully utilized for mushroom cultivation andbiomass production by means of solid-state and submerged liquid fermentation. However,in contrast to submerged liquid fermentation, solid-state fermentation is not often used inlarge scale due to severe engineering problems. Various Pleurotus species have been shownto possess a number of medicinal properties, such as antitumour, immunomodulatory, anti-genotoxic, antioxidant, anti-inflammatory, hypocholesterolaemic, antihypertensive, antipla-telet-aggregating, antihyperglycaemic, antimicrobial and antiviral activities. These thera-peutic activities are exhibited by extracts or isolated compounds from Pleurotus spp. fer-mentation broth, mycelia and fruiting bodies. In particular, polysaccharides appear to bepotent antitumour and immuno-enhancing substances, besides possessing other beneficialactivities. However, the biochemical mechanisms of these therapeutic activities still remainlargely unknown. This review focuses on recent advances in the biotechnology of Pleurotusspp., with emphasis on the production of fruiting bodies, the production of mycelium andbioactive compounds by solid-state and submerged liquid fermentation. The medicinal pro-perties of this mushroom are also outlined. Key words: Pleurotus, mushroom cultivation, biomass production, solid-state fermentation,submerged liquid fermentation, medicinal properties
Introduction
last few decades (1,2); in 1997 it accounted for 14.2 % ofthe total world edible mushroom production (). Its pop-
Cultivation of the oyster mushroom, Pleurotus spp.,
ularity has been increasing due to its ease of cultivation,
has increased greatly throughout the world during the
high yield potential and high nutritional value (3). Al-
*Corresponding author; Phone: ++386 40 756 146; E-mail: andrej.gregori@gmail.com
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
though commonly grown on pasteurized wheat or rice
in soil resulted in a BE of up to 123 % and proved to be
straw, it can be cultivated on a wide variety of lignocel-
the optimal method for P. nebrodensis cultivation (11).
lulosic substrates, enabling it to play an important role
Pleurotus spp. can also colonize and produce mush-
in managing organic wastes whose disposal is problem-
rooms on pretreated conifer (Pinus spp.) wood chips but
they do not always readily colonize non-pretreated coni-
New technologies and production techniques are
fer wood, due to the presence of inhibitory components
being constantly developed as the number of required
(12). Some strains can, however, be adapted for cultiva-
controllable environment parameters increases (4). Cur-
tion on conifer-sawdust-based substrates (13). Pleurotus
rently, solid-state fermentations, other than fruiting body
spp. can also be cultivated on wood waste or unused
production with Pleurotus spp., are used either in the
wood residues associated with harvesting or thinning
transformation of wastes into animal feed or for enzyme
operations, which can enhance economic returns needed
production. Submerged liquid fermentation can, on the
to support ecosystem management (14).
other hand, provide more uniform and reproducible bio-
Some pretreatment or supplementation with nutri-
mass and can prove interesting for valuable medicinal
ents may be necessary. P. ostreatus BE is much lower when
products or for enzyme production because of uncom-
it is cultivated on fresh sawdust than on composted saw-
plicated downstream processing (5). Current research on
dust/bran mixture (15). Rodriguez Estrada and Royse
Pleurotus spp. related to solid-state and submerged li-
(16) reported that P. eryngii fruiting body yields were
quid fermentation is mainly concerned with substrate
significantly higher in substrates containing Mn (50 mg/g)
composition and optimization of culture parameters.
and soybean than in the basal cottonseed hull/sawdust
Pleurotus species have been used by human cultures
all over the world for their nutritional value, medicinal
Different types of straw are commonly used for Ple-
properties and other beneficial effects. Oyster mushrooms
urotus spp. cultivation. Straw can be composted or pas-
are a good source of dietary fibre and other valuable nu-
teurized and extra additives can be used to increase the
trients. They also contain a number of biologically active
BE. When using rice and wheat straw for P. sajor-caju
compounds with therapeutic activities. Oyster mushrooms
cultivation, higher yields were obtained on ground than
modulate the immune system, inhibit tumour growth and
on chopped straw, and yields were 10 % higher on rice
inflammation, have hypoglycaemic and antithrombotic
than on wheat straw. Higher spawn levels enhanced mush-
activities, lower blood lipid concentrations, prevent high
room yields (17). Rice straw appeared to be the best sub-
blood pressure and atherosclerosis, and have antimicro-
strate for P. ostreatus mushroom cultivation when com-
bial and other activities (6). Recent studies of the medic-
pared to banana leaves, maize stover, corn husks, rice
inal properties of oyster mushrooms have focused on
husks and elephant grass (15). When cultivating P. flo-
isolated bioactive compounds; however synergistic ef-
rida, the incorporation of cotton seed powder into rice
fects of the constituents of mushroom extracts may be
straw substrate enhanced mushroom yield, increased net
and total protein, free amino acids and total lipids con-tent, while there was a significant decrease in total di-
Pleurotus spp. Fruiting Body Production
etary fibre, free sugars and polymeric carbohydrates (18). Substrates for oyster mushroom cultivation
Supplementation of rice straw with a residual slurry ob-tained after production of biogas from manure improved
Pleurotus spp. cultivation is a very simple procedure
the yield potential and increased protein and mineral
in the case of log cultivation because it does not involve
contents of P. sajor-caju mushrooms (3). Wheat straw sup-
sophisticated equipment. However, despite its simplic-
plemented with Lolium perenne grass chaff stimulated
ity, large-scale cultivation on natural logs is not often
fructification and mushroom yield of P. pulmonarius (19).
used due to long incubation periods, low yields and en-
P. tuber-regium strains from Australasian-Pacific regions
vironment-dependent production if conducted outdoors.
showed faster mycelium growth rates when cultivated
Yields of P. ostreatus fruiting bodies vary with the spe-
on wheat straw, while wild Nigerian strains performed
cies of trees used and range from 21 % biological effi-
better in sclerotia yield when cultivated on this substrate
ciency (BE) for beech wood to 3 % BE for alder wood
Cultivation of Pleurotus spp. on substrates contain-
Broadleaf hardwood sawdust and straw-based sub-
ing added olive mill waste and wastewaters (OMWW)
strates with added supplements are more often used in
can be a viable alternative for converting these environ-
commercial production. In this case, these artificial sub-
mentally problematic materials into valuable, highly nu-
strates must be pretreated, mainly for elimination of con-
tritious food. It has been shown that wetting a wheat
taminants, and handled in a clean environment. There
straw and bran substrate with OMWW diluted in tap
are different methods of cultivation like shelf, bag, bot-
water (25 %) had no significant negative effect on the
tle, tray, jar, grid-frame, wall-frame and others (8). In
time required for mycelial colonization, primordium ini-
practice, the most used are bag, bottle and shelf cultiva-
tiation or mushroom yield of P. sajor-caju and P. citrino-
tion (9). Evaluation of P. columbinus cultivation in differ-
pileatus. Application of 50 % OMWW led to a delay in
ent bagging systems, in which partially pasteurized of-
colonization and reduction in yield, and deleterious ef-
fice papers were used as a growing substrate, revealed
fects were noted when using 75 % OMWW (21). Sub-
that polyethylene bags resulted in 109 % BE, followed
strates with the addition of OMWW up to 30 % did not
by pottery (86 %), plastic trays (72 %) and polyester net
interfere with mycelial growth of P. pulmonarius but they
(56 %) (10). Removal of the bottom half of the plastic
did inhibit fruiting body formation. OMWW up to 10 %,
cultivation bag and embedding artificial logs vertically
however, did not inhibit pinhead appearance (22). Expe-
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
riments with wild and commercial strains of P. ostreatus,
straw. Sorghum resulted in the lowest mushroom mass
P. eryngii and P. pulmonarius demonstrated significantly
and pileus/stipe ratio, whereas the lowest protein and
higher colonization rates on wheat straw and cotton waste
nitrogen content, and dry material mass were obtained
than on peanut shells. Faster colonization was achieved
with wheat straw (32). Among different agrowastes tested
on non-composted than on composted wheat straw and
(cotton stalk, coir fibre, sorghum stover and mixtures of
cotton waste substrates. Cellulose/lignin ratios in sub-
these wastes), the maximum yields of P. sajor-caju and
strates were positively correlated to mycelial growth rates
P. citrinopileatus were obtained on cotton stalks, while
and mushroom yields of P. ostreatus and P. pulmonarius. P. platypus yields peaked on sorghum stover (33).
In addition, there was a positive correlation between theC/N ratio and P. eryngii mushroom yield (23). A sub-
Weed plants (Leonotis sp., Sida acuta, Parthenium ar-
strate composed of coffee pulp and Digitaria decumbensgentatum, Ageratum conyzoides, Cassia sophera, Tephrosia
was also used for P. ostreatus cultivation and additional
purpurea and Lantana camara) without heat pretreatment
composting of this mixture improved the BE (24). When
were tested for P. ostreatus cultivation. Leonotis sp. mixed
using a mixture of coffee pulp and wheat straw for P. dja-
with rice straw was the best substrate for spawn run
mor, P. ostreatus and P. pulmonarius cultivation, the ob-
and mushroom cultivation while T. purpurea was the least
served decrease in caffeine content of the coffee pulp sam-
appropriate. The main problem of P. ostreatus cultivation
ples during the fruiting stage suggests that some caffeine
on weed-composed substrates was the low yield that
accumulates in the fruiting bodies (25).
was obtained in the second flush. This problem could be
Much effort has been put into optimizing substrates
overcome by mixing weed plants with rice straw. The
based on different grass species for Pleurotus spp. culti-
fruiting body protein content was higher when P. ostrea-
vation. This is an effective way of converting abundant
tus was cultivated on Cassia sophera, Parthenium argenta-
but low value materials into highly nutritional food, es-
tum and Leonotis sp. than on weeds supplemented with
pecially where wood and straw are scarce (26). Lolium
rice straw or on rice straw alone (34). perenne grass chaff stimulated fructification and mush-room yield of P. pulmonarius (19). Wooden crates were
When hazelnut, Tilia spp., European aspen leaves,
used, in a very simple substrate preparation for P. ostrea-
wheat straw, sawdust and waste paper were used as
tus, for composting a mixture of grass (Digitaria decum-
substrates, the best major component and substrate com-
bens) and coffee pulp; 60 and 93 % BE were obtained in
bination for mushroom productivity were wheat straw
two harvests. Further composting for two to three days
and wheat straw in combination with waste paper. Mix-
in each case improved the BE (24). When using chop-
tures involving waste paper generally produced higher
ped, pasteurized switch grass (Panicum virgatum) and
yields than other combinations. The lowest yield and
pasteurized cottonseed hulls with wheat straw for P. cor-
the smallest fruiting body diameters were obtained from
nucopiae cultivation, higher yields were obtained on cot-
Tilia spp. and European aspen leaves in combination
tonseed hulls/wheat straw substrate. Increasing spawn
with sawdust. The greatest number of fruiting bodies
and supplement levels in switch grass/wheat straw sub-
was obtained on a mixture of wheat straw, hazelnut
strate stimulated yield in a linear fashion. However, ma-
leaves and waste paper (35). Mandeel et al. (10) culti-
ximum yields were less than 50 % of those obtained with
vated Pleurotus spp. on various lignocellulosic wastes
cottonseed hulls/wheat straw substrate (27). When sup-
supplemented with fresh chicken manure. The highest
plementing spent rice straw substrate with oil seed cakes,
BE was noted on cardboard with both P. columbinus (134
cottonseed powder proved best in enhancing P. sajor-
%) and P. ostreatus (117 %). Experiments conducted by
-caju mushroom yields. Mushrooms grown on substrate
Baysal et al. (36), which involved cultivation of P. ostrea-
supplemented with cottonseed powder had increased
tus on waste paper with addition of chicken manure,
protein and fat content, decreased carbohydrate content
peat and rice husks, showed that increasing the amount
and contained no residues of gossypol. In addition, there
of rice husks added to the substrate accelerated spawn
was a significant reduction in the spawn run period when
running, pinhead formation and fruiting body forma-
compared to the use of unsupplemented rice straw (28).
tion. Larger proportions of peat and chicken manure had
P. ostreatus and P. sajor-caju exhibited higher ash con-
a negative effect on growth. A study on growth and pro-
tent when cultivated on rice straw than when cultivated
ductivity of different P. ostreatus strains on sunflower
on banana straw, and P. sajor-caju also showed higher
moisture and fibre content when cultivated on rice straw
that the addition of growth-limiting mineral nutrients
(29). When cultivating P. ostreatus on corn and pumpkin
increased the mycelial growth rate. BE increased over
straw, the substrate had no effect on the nitrogen con-
control values and reached 60–112 %, depending on the
tent and amino acid profile of the fruiting bodies; how-
strain and the concentration of Mn and N–NH +
ever, the nitrogen content increased from the first har-vest to the third harvest (30). Using water hyacinth biomass
Non-pretreated spent brewery grains were success-
as substrate, BE was found to be higher with P. florida
fully used as a basic substrate material for P. ostreatus
(86 %) than with P. citrinopileatus (79 %) (31). When P.
cultivation in polypropylene bottles. Few fruiting bodies
ostreatus var. salignus was cultivated on peanut, soybean,
were formed on spent grain alone; however 19 % BE
sorghum or wheat straw, the highest and lowest yields
was obtained with the addition of 45 % wheat bran. The
were obtained on peanut and sorghum straw, respec-
chemical analysis of fruiting bodies indicated that P. os-
tively. The highest protein content, pileus/stipe ratio,
treatus cultivated on spent grain substrate had a higher
sporophore mass, percentage of dry material, and nitro-
nutritional value than those grown on other types of sub-
gen and carbon contents were obtained with peanut
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
Other factors influencing oyster mushroom
for vigorous P. nebrodensis growth were glucose, peptone
There have been various reports on other factors that
Mycelium production on lignocellulosic substrates
influence the development of oyster mushrooms. None
has also been investigated. Amongst seven mushroom
of these factors has been studied in depth; the various
cultivation substrates, the mycelial extension rates were
observations that have been made are outlined in the pa-
highest on cotton gin-trash, peanut shells and poplar
sawdust. Supplemented oak sawdust and olive millwaste were poor substrates for most species examined,
Cho et al. (39) discovered that inoculation of pure
while almost all strains performed adequately on corn
P. ostreatus mycelium cultures with strains of fluorescent
cobs (44,45). Different substrate combinations were eval-
Pseudomonas spp., isolated from the mycelial plane of
uated for P. ostreatus mycelial growth and favourable
commercially produced mushrooms, promoted the for-
combinations were Tilia spp. leaves with wheat bran
mation of primordia and enhanced the development of
and Populus spp. leaves with wheat straw. The authors
the basidiomata. These results strongly suggest that in-
also reported that mycelial growth and mushroom yield
oculation of the mycelium with specific bacteria may
have different requirements (46), whereas others re-
have beneficial applications for mushroom production.
ported that mushroom yield was directly related to the
It was reported that the bacterial blotch disease in
spread of the mycelium within the substrate (15).
mushrooms caused by Pseudomonas tolaasii was more se-vere when substrates were amended with Cu in P. eryngiiSSF waste utilization and enzyme production by
cultivation (16). Two compounds from olive mill waste,4-methylcatechol and catechol, were found to be effective
against P. tolaasii and supplementation with up to 10 %
Much work has been done recently on waste utiliza-
OMWW reduced bacterium-related symptoms (22).
tion by Pleurotus spp., mostly concerned with the poten-
Qu et al. (40) demonstrated the influence of heavy
tial of locally available waste and agricultural by-prod-
metals in substrates on P. eryngii primordial formation,
ucts for either transformation into animal feed or as
fruiting body development and BE. Heavy metal (As,
primary substrates for enzyme production.
Hg, and Cd) supplementation decreased average growth
Villas-Bôas et al. (47) investigated the conversion of
yields and BE of P. eryngii, whereas Pb supplementation
apple pomace by Candida utilis and P. ostreatus, sepa-
rately and in coculture, in SSF. C. utilis was a better can-
Irradiation by red and green light stimulated vege-
didate for biological treatment of apple pomace as the
tative growth of P. ostreatus mycelium and shortened the
yeast lowered the residual free sugar concentration more
substrate colonization and fructification time. The in-
than P. ostreatus did. When both organisms were used,
creased fruiting body yield in irradiated cultures reached
apple pomace digestibility decreased while the protein
content increased, with the final product being suitablefor use as a protein supplement for cattle feed. Fermen-
The cytolytic protein ostreolysin, isolated from P. os-
tation with P. ostreatus alone was, however, discarded as
treatus fruiting bodies, was specifically expressed during
a viable treatment of apple pomace. Furthermore, recy-
fruiting initiation, suggesting its involvement in fruiting
cling of viticulture waste in SSF with P. ostreatus and
body formation. When purified ostreolysin was used as
P. pulmonarius also yielded a high-fibre feed for limited
a supplement on nutrient media plates inoculated with
use in ruminants (48). Tests on water hyacinth biomass
P. ostreatus mycelium, the protein stimulated primordia
delignification showed that organic matter loss was
and fruiting body formation (42).
higher in samples inoculated with P. citrinopileatus thanP. florida. Improvement of delignification and dry matter
Solid-State Fermentation with Pleurotus spp.
digestibility was, however, higher with P. florida, whichalso proved to be more effective than P. citrinopileatus for
Most solid-state fermentations (SSF) with Pleurotus
the production of highly digestible mycoprotein-rich ru-
spp. have been small scale, that is, they have involved
minant feed (31). Intensive P. ostreatus mycelial growth
solid substrate in Erlenmeyer flasks or in agar plates.
was observed in substrates containing leftover hemp
Recent studies have been focused on the utilization of
seeds, whole ground corn plant or sesame oil press cake.
lignocellulosic organic waste materials for either lignin
Intermediate growth was observed in substrates con-
degradation, use as animal feed or enzyme production.
taining olive mill waste, rape oil press cake or sunfloweroil press cake while slowest growth rates were observedin the substrate containing soy oil press cake (44,45). SSF for Pleurotus spp. mycelial biomass and
Ghibom et al. (49) introduced a novel approach for uti-
lizing whey permeate with P. ostreatus in an SSF system.
When agar-based media are used, medium compo-
They concluded that whey permeate could provide a vi-
sition plays an important role as it determines the my-
able substrate for production of P. ostreatus mycelium.
celial growth rate, and correct medium ingredient ratios
The optimal growth conditions were 44 g/L lactose,
are crucial for fast colonization. Nasim et al. (43) found
that malt extract agar (MEA) provided faster P. ostreatus
White-rot basidiomycetes are efficient decomposers
mycelial growth rates than did Murashige and Skoog’s
of lignocellulose, due to their capability to synthesize
(MS) medium and potato dextrose agar (PDA). The slow-
relevant hydrolytic and oxidative extracellular enzymes.
est growth was observed on PDA medium. The most ef-
Lignocellulolytic enzymes have significant potential ap-
fective carbon, nitrogen and inorganic salt supplements
plications not only in the chemical, fuel, food, textile,
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
laundry and pulp and paper industries but also in agri-
as liquid spawn for fruiting body production on solid
culture and for animal feed production (50).
substrates; biomass production for food, dietary supple-
Hölker and Lenz (4) introduced a trickle-film fer-
ment and pharmaceutical applications; and conversion
mentation process on sugarcane bagasse with P. ostreatus
of waste biomass and enzyme production. SLF offers the
for laccase production, which turned out to be highly
possibility of high biomass production in a compact
suitable for extracellular enzyme production. High en-
space, shorter time and with fewer chances of contami-
zyme levels were produced when the growth medium
nation (57,58). While SSF will remain the chosen method
was repeatedly changed. When compared to submerged
for mushroom production, there will be a continued in-
liquid fermentation, the productivity was better and two
crease in the development of SLF technology to produce
more uniform and reproducible biomass of medicinal
Banana leaf waste was a better substrate than ba-
fungi. Western biotechnology companies have yet to rec-
nana pseudostem waste in the production of extracellu-
ognize the potential in this area of medical bioscience
lar enzymes by P. ostreatus and P. sajor-caju in SSF and is
a potential alternative to other agrowaste substrates. Theyields were, however, too low and commercially not vi-
SLF for Pleurotus spp. biomass and polysaccharide
able. It was suggested that a larger surface area of ba-
nana leaf waste could be a determining factor for betterenzyme production (51). This is in agreement with Zhang
The most detailed study of P. ostreatus growth in SLF
et al. (17) who reported that P. sajor-caju grew faster and
was conducted by Márquez-Rocha et al. (59). They stud-
provided better yields on ground straw than on chopped
ied P. ostreatus cultivation in a stirred tank bioreactor
straw. There is, however, a substrate particle size limit,
and revealed that by varying impeller geometry and
as more finely ground straw inhibited growth. Optimal
speed, and aeration intensity, the growth rate and pellet
particle sizes should therefore be determined for all ap-
size changed. A clear tendency was observed for smaller
pellet sizes to result in higher specific growth rates. For
Staji} et al. (52) performed SSF with Pleurotus spp.
promotion of mycelium growth the pellets need to be
on grapevine sawdust, which was supplemented with
broken down, but on the other hand, a balance between
synthetic medium to provide nitrogen and trace miner-
growth and hyphal fragmentation must also be achieved.
als. Peroxidase activity was detected in all strains evalu-
The lag phase for P. tuber-regium growth and biocon-
ated, the highest being with P. ostreatus and P. pulmo-
version efficiency in SLF was shorter with glucose and
narius. The highest laccase activity was detected at 10
fructose than with maize starch. In scaled-up fermenta-
days of fermentation in P. ostreatus followed by P. pulmo-
tions, addition of fructose to basal medium supported
narius and P. eryngii. Organic nitrogen sources have been
higher mycelial yields than the addition of glucose. Yeast
shown to stimulate enzyme production more than inor-
extract as the nitrogen source proved better than pep-
ganic sources. Cyanobacterial biomass was used as a ni-
tone when monosaccharides were used as the sole car-
trogen supplement and stimulated P. ostreatus growth and
laccase production in SSF. The authors concluded that
Recent studies on mushroom polysaccharides have
dry biomass of diazotrophic cyanobacteria not only helps
demonstrated many interesting biological activities, which
to maintain an optimal C/N ratio but also confers a
are described later in this review. The production of Pleu-
good porosity, which sustains the oxygen supply within
rotus spp. mycelial biomass and valuable polysaccharides
the matrix of solid particles (53). The nature of the sub-
in SLF depends on the species used, growth parameters,
strate as well as the cultivation method affects the ex-
growth timing and their nutritional requirements (61,62).
pression of lignocellulolytic enzymes. The study con-
Response surface methodology, a widely known optimi-
ducted by Elisashvili et al. (54) revealed that SSF of tree
sation procedure, was used to optimise the medium in
leaves by Pleurotus spp. was favourable for laccase and
order to maximize growth and polysaccharide produc-
manganese peroxidase (MnP) production. Furthermore,coculturing can be an effective method for biopulping
tion by P. citrinopileatus. The highest polysaccharide yield
and improvement of lignin degradation (55,56). Chi et al.
was obtained with a C/N ratio of 40, an initial pH=5.5
(56) demonstrated that coculturing P. ostreatus with Ceri-
and a cultivation temperature of 25 °C (63). Another pa-
poriopsis subvermispora significantly stimulated lignin de-
rameter that influenced growth and polysaccharide pro-
gradation when compared to monocultures. Laccase pro-
duction by P. ostreatus in SLF was the initial oxygen
duction and MnP activity were stimulated in cocultures
transfer rate (KLa). Better polysaccharide yields were ob-
of P. ostreatus with C. subvermispora or Physisporinus rivu-
tained with a lower initial KLa (64). losus and a change in the isoform composition of thoseenzymes was also observed. Waste utilization and enzyme production by
These studies show that the cultivation method can
have drastic effects on the production of valuable sub-
SLF is also suitable for enzyme production and waste
stances by Pleurotus spp. and its economical feasibility.
bioconversion. Most recent work is focused on substrateoptimization for maximal production of hydrolytic and
Submerged Liquid Fermentation with
oxidative ligninolytic extracellular enzymes. Pleurotus spp.
Staji} et al. (52) performed SLF with P. eryngii, P. os-treatus and P. pulmonarius on different carbon and nitro-
Submerged liquid fermentation (SLF) techniques
gen sources. In the medium with the best carbon sources
have been developed for a variety of fungi and are used
(mandarin peels and grapevine sawdust), both P. eryngii
in mycelium propagation for different applications, such
and P. ostreatus showed the highest laccase activity with
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
(NH4)2SO4 as the nitrogen source. With P. ostreatus and
P. pulmonarius, the best nitrogen sources for productionof peroxidases were peptone and NH
Much recent research has been carried out on
composition of the cultivation medium is important for
Pleurotus spp. extracts and isolated compounds such as
good enzyme production and various inducers have been
polysaccharides, proteins and other substances that pos-
tested for stimulating P. ostreatus enzyme production. Hou
sess antineoplastic activities in vitro and in vivo. et al. (65) obtained high levels of laccase activity using
Various crude extracts of Pleurotus species have been
cellobiose and peptone as the carbon and nitrogen sour-
shown to possess relatively strong antitumour activities.
ces. 2,2’-Azino-di-(3-ethylbenzothialozin-6-sulphonic
Methanol extracts of P. florida and P. pulmonarius fruiting
acid) (ABTS) and Cu had a positive effect on laccase pro-
bodies significantly reduced solid tumours in mice (70,71).
duction and the former was shown to be the best laccase
P. ostreatus mycelium extract, alone and combined with
inducer in their study. Static cultures were superior to
the chemotherapeutic agent cyclophosphamide, inhibited
agitated cultures in terms of growth and laccase produc-
in vivo tumour growth in mice. The combined adminis-
tion, while nitrogen-limited culture media were only be-
tration of the extract with cyclophosphamide decreased
neficial for laccase production. In another study, the
the degree of leukopenia compared to administration of
Taguchi orthogonal array experimental design was ap-
cyclophosphamide alone (72). A water extract of P. ostre-
plied for the optimization of laccase production in SLF
atus exhibited the most significant cytotoxicity by induc-
with P. ostreatus. The most influential factor for laccase
ing apoptosis of human carcinoma cells, when compared
production was found to be the inducer 2,5-xylidine, fol-
to many other mushroom extracts. It has been suggested
lowed by glucose concentration, wheat bran content, urea
that the active compounds in the extract were water-sol-
concentration, inoculum size, yeast extract concentration
uble proteins or polypeptides (73).
and pH (66). Mikiashvili et al. (67) reported that the high-est MnP and laccase activities were obtained in xylan-
Among the components of such extracts, polysaccha-
-supplemented media, but enzyme activities decreased
rides are well-documented as potent antitumour and
when supplemented with inorganic nitrogen sources.
immunomodulating substances (74,75). Many polysac-
Peptone, followed by casein, was used as the nitrogen
charides from Pleurotus spp. have been isolated and
source for the best laccase accumulation; this results be-
identified (76–86). For some of them, important medici-
ing attributable to higher biomass production. MnP and
nal properties, including antitumour activities, have been
peroxidase secretion was stimulated by supplementation
shown. P. tuber-regium polysaccharides, extracted from
with casein hydrolysate. A liquid medium composed of
mycelium and fruiting bodies, effectively inhibited solid
mandarin peels and leaves inoculated with P. dryinus al-
tumour proliferation in mice. Antitumour effects have also
lowed the simultaneous production of hydrolases and oxi-
been shown on different human tumour cell lines (87,88).
dases at high levels. Carboxymethyl cellulase and xyla-
Wong et al. (89) showed that P. tuber-regium polysaccha-
nase appeared to be inducible enzymes. Addition of Mn
rides exerted antitumour activity, through cytotoxicity and
enabled the laccase to MnP ratio to be regulated. For MnP
antiproliferative activity, against human leukaemia cells
production the presence of lignocellulosic substrates is a
in vitro. The polysaccharides induced apoptosis and caused
prerequisite and shows a positive correlation with their
cell-cycle arrest. Compared to native P. tuber-regium po-
addition (50). This is supported by Hou et al. (65), who
lysaccharides, their corresponding carboxymethylated or
did not detect any MnP activity in N limited glucose me-
sulphated derivatives showed higher antitumour activ-
dium with P. ostreatus. Pleurotus spp. SLF on tree leaves
ity, presumably because of their higher water solubility
provided better hydrolytic enzyme production than SSF
and relatively extended flexible chains (90–93). A novel
a-glucan from P. ostreatus mycelium induced apoptosis
P. ostreatus mycelium could be cultivated employing
of colon cancer cells in vitro (94) and water-soluble poly-
coffee pulp wastewater extract supplemented with glu-
saccharides extracted from P. citrinopileatus fermentation
cose. The polluting load was reduced by more than 50
broth have been shown to reduce the number of meta-
% at the end of 20 days of fermentation (68). SLF with
static tumour nodules in tumour-bearing mice (63). P. ostreatus was also used for removing phenolic com-
Antitumour properties have also been demonstrated
pounds from olive oil mill wastewater (OMWW). Lac-
for Pleurotus spp. proteins, proteoglycans, and DNA. A
case was the sole ligninolytic enzyme detected and was
lectin isolated from P. ostreatus potently inhibited growth
produced during primary growth. The phenolic content
of sarcoma and hepatoma in mice and prolonged their
and toxicity were successfully reduced, but only when
lifespan (95). A P. eous lectin exerted antiproliferative ef-
high OMWW dilutions were used. This could be a valu-
fects on human tumour cell lines while showing no cy-
able method for problematic OMWW treatment before
totoxicity (96). Furthermore, two ribonucleases isolated
its release into the environment (69).
from P. sajor-caju and P. ostreatus fruiting bodies exhib-ited antiproliferative effects on tumour and leukaemia
Medicinal Properties of Pleurotus spp.
cell lines (97,98). Another protein, eryngeolysin, isolatedfrom P. eryngii fruiting bodies, exhibited cytotoxicity
Recent studies on various Pleurotus species have
against leukaemia cells (99). Water-soluble proteoglycans
shown a number of therapeutic activities, such as anti-
were purified from P. ostreatus mycelium and exerted anti-
tumour, immunomodulatory, antigenotoxic, antioxidant,
tumour activity in sarcoma-bearing mice. Proteoglycans
anti-inflammatory, hypocholesterolaemic, antihyperten-
injected into mice reduced the number of tumour cells
sive, antiplatelet-aggregating, antihyperglycaemic, antimi-
by cell cycle arrest (100). Moreover, DNA isolated from
P. ostreatus fruiting bodies administered to mice with
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
solid Ehrlich carcinoma significantly increased the life-
trate, presumably due to a higher amount of total phe-
nols. Methanol extracts of P. florida and P. pulmonariusfruiting bodies showed similar antioxidant activities
Immunomodulatory and antimitogenic activities
(70,71), and an ethanol extract from P. citrinopileatus frui-ting bodies had antioxidant activities comparable to those
The antitumour effects of mushrooms are mostly at-
from P. eryngii, P. ferulae and P. ostreatus mushrooms
tributed to stimulation of the immune response. Re-
cently, several compounds from Pleurotus species withimmunostimulatory activities on humoral and cell-medi-
P. citrinopileatus fruiting body extracts have shown
ated immunity have been isolated. Water-soluble poly-
antioxidant activities in vitro and in hyperlipidaemic
saccharides extracted from Pleurotus citrinopileatus fermen-
hamster rats. Extracts added to a high-fat diet increased
tation broth administered to mice resulted in a signifi-
the activities of antioxidant enzymes in rats (113). P. ostrea-
cant increase in the number of macrophages, T, CD4+
tus mushroom extracts had antioxidant properties in
and CD8+ cells (63). Glucans isolated from P. florida frui-
aged and CCl4-induced liver damaged rats, as indicated
ting bodies activated the phagocytic response of mouse
by significant increases in concentrations of antioxidants
macrophages in vitro (83) and significantly induced the
and antioxidant enzymes (114,115). Pleuran, a b-glucan
proliferative response as well as phagocytic activity of
isolated from P. ostreatus, had a positive effect on the an-
fish leukocytes in vitro (102). Moreover, proteoglycans
tioxidant status of rats and decreased precancerous le-
from P. ostreatus mycelia exerted immunomodulatory ef-
sions induced in rat colon (116). A polysaccharide-pep-
fects by elevating mouse natural killer cell cytotoxicity
tide complex isolated from P. abalonus fruiting bodies
and by macrophage stimulation (100). DNA isolated
prolonged the lifespan of senescence-accelerated mice.
from P. ostreatus fruiting bodies stimulated mouse natu-
Gene expression of antioxidant enzymes was up-regu-
ral killer cytotoxic activity in vitro (101).
lated and consequently their activities were increased(117).
Antimitogenic effects of Pleurotus spp.-derived com-
pounds on immune cells have also been reported. A ri-
bonuclease isolated from P. sajor-caju fruiting bodies ex-erted antiproliferative effect on murine splenocytes (97),
Jose et al. (71,118) showed that methanol extracts of
while eryngeolysin from P. eryngii inhibited the stimu-
P. pulmonarius and P. florida fruiting bodies decreased in-
lated mitogenic response of murine splenocytes (99). Fur-
duced paw oedema in mice and ameliorated acute and
thermore, P. flabellatus lectin did not exhibit any mito-
chronic inflammation, respectively. Pleuran has also been
genic activity towards mouse T cells (103).
shown to possess anti-inflammatory activity by exertingantioxidant and immunomodulatory effects on rats with
Antioxidant and gene protective activities
Hypersensitive immune responses, such as inflam-
Antioxidant compounds prevent oxidative damage
mation in delayed allergy, were suppressed by an etha-
related to aging and diseases, such as atherosclerosis, di-
nol extract of P. eryngii. It exhibited anti-allergic activity
abetes, cancer and cirrhosis. Mushrooms that contain an-
after oral or percutaneous administration to mice with
tioxidants or increase antioxidant enzyme activity may
oxazolone-induced type IV allergy (121).
be used to reduce oxidative damage in humans (104).
Of 89 mushroom species tested, an extract from
Cardiovascular disease protection andP. cornucopiae possessed the most effective antigenotoxic
and bio-antimutagenic activities when tested on Salmo-nella typhimurium and Escherichia coli (105). Furthermore,
Oyster mushrooms possess bioactive compounds with
P. cornucopiae extracts significantly reduced H
hypocholesterolaemic activities, such as polysaccharides,
DNA damage in Chinese hamster lung cells (106) and
mevinolin and other statins (122). It has recently been
P. ostreatus extract mitigated genotoxicity, as shown by
reported that P. citrinopileatus fruiting body extracts ex-
the fact that it suppressed DNA damage induced by va-
erted antihyperlipidaemic effects. Serum triglyceride and
rious mutagens in the Drosophila DNA repair test (107).
total cholesterol levels were lowered in hyperlipidaemic
On the other hand, a water extract of P. sajor-caju fruit-
rats supplemented with the extracts, while high-density
ing bodies had no genoprotective effects since it did not
lipoprotein levels were significantly increased (113). Si-
milar effects were noted when powdered P. ostreatus
2O2-induced oxidative damage to cellular DNA
fruiting bodies or a water-soluble polysaccharide ex-
Methanol extracts of P. ostreatus and P. cystidiosus
tracted from P. citrinopileatus fermentation broth were
fruiting bodies possessed antioxidant, reducing power,
fed to hypercholesterolaemic or diabetic rats, respec-
radical scavenging and iron chelating activities that were
higher than those of other commercial mushrooms (104). Pleurotus species also possess blood-pressure-lower-
On the other hand, Elmastas et al. (109) and Dubost et al.
ing activity. Recently, P. cornucopiae has exhibited antihy-
(110) reported that oyster mushroom extracts possessed
pertensive activity; this might be due in part to D-man-
only moderate antioxidant activities compared to other
nitol, which inhibits angiotensin I converting enzyme
edible mushrooms. The antioxidant activity was posi-
tively correlated with total polyphenol content. Further-
A methanol extract of P. florida fruiting bodies sig-
more, Lee et al. (111) showed that P. citrinopileatus ex-
nificantly inhibited platelet aggregation. The antiplatelet-
tracts prepared from fruiting bodies were more effective
-aggregating activity, along with the anti-inflammatory
than those from mycelium and fermentation broth fil-
activities discussed above, suggest its potential therape-
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
utic use against vascular disorders, but the exact mecha-
food and valuable compounds. These and many other
nism of these activities is unknown (118).
materials have been successfully used for biomass pro-
Antihyperglycaemic activity was demonstrated with
a water-soluble polysaccharide from P. citrinopileatus fer-
Solid- and liquid-state fermentations can be success-
mentation broth. The polysaccharide was effective in
fully applied for Pleurotus spp. cultivation. Each one has
lowering blood glucose levels in diabetic rats (124).
its advantages and shortcomings and the decision as towhich method should be used for a specific application
must be carefully evaluated, as the outcomes are influ-
Antibacterial and antifungal activities have been ob-
enced by several factors. Solid-state fermentation is still
served in Pleurotus spp. extracts and isolated compounds,
the preferred method for waste utilization. Different ap-
presumably produced as a defence mechanism against
proaches can be used for enzyme production, as an ex-
other organisms. Table 1 (126–129) summarizes recently
ample, the trickle film process for laccase production de-
reported antimicrobial activities of Pleurotus spp.
veloped by Hölker and Lenz (4). On the other hand,submerged liquid fermentations can be more uniform
and reproducible, which is interesting for obtaining pro-ducts with medicinal properties, although this potential
Mushrooms contain substances that exert direct or
has yet to be recognized by western biotechnology com-
indirect antiviral effects as a result of immunostimula-
panies (5). Different substrates for solid- and liquid-state
tory activity (130). Inhibitory activity against human im-
fermentations with Pleurotus spp. have been evaluated
munodeficiency virus (HIV)-1 reverse transcriptase has
and nutritional requirements and culturing parameters
recently been demonstrated for P. sajor-caju and P. pul-
were established. The authors point out that the correct
monarius hot water extracts (131). Anti-HIV activity was
selection of medium composition and environmental pa-
also demonstrated for a ubiquitin-like protein isolated from
rameters is crucial if optimal biomass, enzyme or metab-
P. ostreatus fruiting bodies (132). Moreover, Zhang et al.
(133,134) demonstrated that, in contrast to water-insolu-ble b-glucans isolated from P. tuber-regium sclerotia, their
Pleurotus species possess a number of beneficial me-
corresponding water-soluble sulphated derivatives exert
dicinal properties, such as antitumour, immunomodula-
antiviral activities against herpes simplex virus type 1
tory, antigenotoxic, antioxidant, anti-inflammatory, anti-
and type 2. The effect is presumably elicited by the bind-
-allergic, hypocholesterolaemic, antihypertensive, anti-
ing of sulphated b-glucans to viral particles, thus pre-
hyperglycaemic, antimicrobial and antiviral activities.
venting them from infecting the host cells.
These activities have been reported for various extractsand isolated compounds, such as polysaccharides, poly-saccharide-protein complexes, proteoglycans, proteins
Concluding Remarks
and DNA from oyster mushroom fermentation broth,mycelia or fruiting bodies. In particular, polysaccharides
Much work has been carried out on Pleurotus spp.
appear to be potent antitumour and immunomodulating
mushroom cultivation, biomass production by means of
substances, besides possessing other beneficial activities.
solid- and liquid-state fermentation, and medicinal pro-
However, the biochemical mechanisms of these thera-
perties. Studies on mushroom cultivation have been fo-
peutic activities still remain largely unknown.
cused on optimization of alternative substrates. It has beenshown that a wide variety of agricultural (by-)products,weeds and wastes can be successfully used to produce
food, feed, enzyme and medicinal compounds and todegrade and detoxify wastes. Due to an increasingly
We thank the Slovenian Research Agency (applica-
negative human impact on the environment, these tech-
tive research project L2-7598 and L4-6420) that enabled
niques, together with others, constitute a very important
us to write this review article. We would also like to
tool for converting abundant quantities of waste materi-
thank Prof. Dr. Roger Pain for taking the time to review
als, which often cause environmental pollution, into
Table 1. Reported antimicrobial activities of Pleurotus spp.
Gram-positive, Gram-negative bacteria and
Hexane-dichloromethane extract containing
Bacillus subtilis, Pseudomonas aeruginosa, Aspergillusniger and Fusarium oxysporumBacillus spp., Escherichia coli, Vibrio cholerae and
Fusarium oxysporum and Mycosphaerella arachidicolaFusarium oxysporum, Mycosphaerella arachidicola,
Pseudomonas aeruginosa and Staphylococcus aureus
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
References 20. O.S. Isikhuemhen, F. Nerud, R. Vilgalys, Cultivation stu-
dies on wild and hybrid strains of Pleurotus tuber-regium(Fr.) Sing. on wheat straw substrate, World J. Microbiol. Bio-1. S.T. Chang, World production of cultivated and medicinal
technol. 16 (2000) 431–435.
mushrooms in 1997 with emphasis on Lentinus edodes (Berk)
21. E. Kalmis, S. Sargin, Cultivation of two Pleurotus species
Sing, China, Int. J. Med. Mush. 1 (1999) 291–300.
on wheat straw substrates containing olive mill waste wa-
2. D.J. Royse, Influence of spawn rate and commercial de-
ter, Int. Biodeter. Biodegr. 53 (2004) 43–47.
layed release nutrient levels on Pleurotus cornucopiae (oys-
22. C. Soler-Rivas, A. Garcia-Rosado, I. Polonia, G. Junca-
ter mushroom) yield, size and time to production, Appl.
-Blanch, F.R. Marin, H.J. Wichers, Microbiological effects
Microbiol. Biotechnol. 58 (2002) 527–531.
of olive mill waste addition to substrates for Pleurotus pul-3. S. R. Effect of supplementation of rice straw with biogas
monarius cultivation, Int. Biodeter. Biodegr. 57 (2006) 37–44.
residual slurry manure on the yield, protein and mineral
23. A. G. P. Diamantopoulou, Bioconversion of agricultural
contents of oyster mushroom, Ind. Crops Prod. 20 (2004)
lignocellulosic wastes through the cultivation of the edible
mushrooms Agrocybe aegerita, Volvariella volvacea and Pleu-4. U. Hölker, J. Lenz, Trickle-film processing: An alternative
rotus spp., World J. Microbiol. Biotechnol. 17 (2001) 191–200.
for producing fungal enzymes, BIOforum Europe, 6 (2004)
24. D. Hernández, J.E. Sánchez, K. Yamasaki, A simple proce-
dure for preparing substrate for Pleurotus ostreatus cultiva-
5. J.E. Smith, N.J. Rowan, R. Sullivan, Medicinal mushrooms:
tion, Bioresour. Technol. 90 (2003) 145–150.
A rapidly developing area of biotechnology for cancer the-
25. D. Salmones, G. Mata, K.N. Waliszewski, Comparative cul-
rapy and other bioactivities, Biotechnol. Lett. 24 (2002) 1839–
turing of Pleurotus spp. on coffee pulp and wheat straw:
Biomass production and substrate biodegradation, Biore-6. N. Gunde-Cimerman, Medicinal value of the genus Pleu-sour. Technol. 2005) 537–544. rotus (Fr.) P. Karst. (Agaricales s.l., Basidiomycetes), Int. J.26. L. Zhanxi, L. Zhanhua: JUNCAO Technology, China Agri-
cultural Scientech Press, Beijing, China (2001) pp. 131–134,
, Growing of Pleurotus ostreatus on woods of vari-
ous deciduous trees, Acta Edulis Fungi, 12 (2005) 306–312. 27. D.J. Royse, T.W. Rhodes, S. Ohga, J.E. Sanchez, Yield, mush-
8. P. Stamets: Growing Gourmet and Medicinal Mushrooms, Ten
room size and time to production of Pleurotus cornucopiae
Speed Press, Berkeley, USA (2000) p. 150.
(oyster mushroom) grown on switch grass substrate spaw-ned and supplemented at various rates, Bioresour. Technol.9. K.W. Choi, Oyster mushroom cultivation: Shelf or bag?
(2003) (http://www.mushworld.com). 28. M.N. Shashirekha, S. Rajarathnam, Z. Bano, Enhancement
10. Q. Cultivation of oyster mushrooms (Pleurotus spp.) on va-
of bioconversion efficiency and chemistry of the mush-
rious lignocellulosic wastes, World J. Microbiol. Biotechnol.
room Pleurotus sajor-caju (Berk and Br.) Sacc. produced on
spent rice straw substrate, supplemented with oil seed
11. H.D. Guo, L.Z. Wan, C.Y. Huang, Y.C. Yu, B.S. Zhang, H.T.
cakes, Food Chem. 76 (2002) 27–31.
Shan, Effect of nutritional parameters and temperature on
29. M. Bonatti, P. Karnopp, H.M. Soares, S.A. Furlan, Evalua-
the growth of Pleurotus nebrodensis mycelium, and an opti-
tion of Pleurotus ostreatus and Pleurotus sajor-caju nutritio-
mized cultivation method, Acta Edulis Fungi, 13 (2006) 71–
nal characteristics when cultivated in different lignocellu-
losic wastes, Food Chem. 88 (2004) 425–428. 12. S.C. Croan, Conversion of conifer wastes into edible and
30. L. Ancona Mendez, C.A. Sandoval Castro, R. Belmar Casso,
medicinal mushrooms, Forest Prod. J. 54 (2004) 68–76.
C.M. Capetillo Leal, Effect of substrate and harvest on the
13. R.G. Ruan, L.C. Ding, X.H. Pan, H. Chen, Y.F. Luo, Dome-
amino acid profile of Oyster mushroom (Pleurotus ostrea-
stication and cultivation of Pleurotus citrinopileatus strain
tus), J. Food Compos. Anal. 18 (2005) 447–450.
Ninghuang No. 16 on a substrate containing pine and fir
31. R. Mukherjee, B. Nandi, Improvement of in vitro digest-
sawdust, Acta Edulis Fungi, 13 (2006) 36–38.
ibility through biological treatment of water hyacinth bio-
14. S.C. Croan, Conversion of wood waste into value-added
mass by two Pleurotus species, Int. Biodeter. Biodegr. 53
products by edible and medicinal Pleurotus (Fr.) P. Karst.
species (Agaricales s.l., Basidiomycetes), Int. J. Med. Mush.32. A. Yildiz, M. Karakaplan, F. Aydin, Studies on Pleurotusostreatus (Jacq. ex Fr.) Kum. var. salignus (Pers. ex Fr.)
15. M. Obodai, J. Cleland-Okine, K.A. Vowotor, Comparative
Konr. et Maubl.: Cultivation, proximate composition, orga-
study of the growth and yield of Pleurotus ostreatus on dif-
nic and mineral composition of carpophores, Food Chem.
ferent lignocellulosic by-products, J. Ind. Microbiol. Biotech-33. R. Ragunathan, K. Swaminathan, Nutritional status of Ple-16. A.E. Rodriguez Estrada, D.J. Royse, Yield size and bacte-
urotus spp. grown on various agro-wastes, Food Chem. 80
rial blotch resistance of Pleurotus eryngii grown on cotton-
seed hulls/oak sawdust supplemented with manganese,
34. N. Das, M. Mukherjee, Cultivation of Pleurotus ostreatus on
copper and whole ground soybean, Bioresour. Technol. (2007)
weed plants, Bioresour. Technol. 98 (2007) 2723–2726. 35. S. Yildiz, Ü.C. Yildiz, E.D. Gezer, A. Temiz, Some ligno-
17. R. Zhang, X. Li, J.G. Fadel, Oyster mushroom cultivation
cellulosic wastes used as raw material in cultivation of the
with rice and wheat straw, Bioresour. Technol. (2002) 277–
Pleurotus ostreatus culture mushroom, Process Biochem. 3818. M.N. Shashirekha, S. Rajarathnam, Z. Bano, Effects of sup-
36. E. Baysal, H. Peker, M. K. Yalinkiliç, A. Temiz, Cultivation
plementing rice straw growth substrate with cotton seeds
of oyster mushroom on waste paper with some added sup-
on the analytical characteristics of the mushroom, Pleuro-
plementary materials, Bioresour. Technol. 89 (2003) 95–97. tus florida (Block & Tsao), Food Chem. (2005) 255–259. 37. N.R. Curvetto, D. Figlas, R. Devalis, S. Delmastro, Growth
19. D.L. Domondon, W. He, N.D. Kimpe, M. Höfte, J. Poppe,
and productivity of different Pleurotus ostreatus strains on
-Adenosine, a bioactive compound in grass chaff stimu-
sunflower seed hulls supplemented with N–NH + and/or
lating mushroom production, Phytochemistry, 65 (2004) 181–
Mn(II), Bioresour. Technol. 84 (2002) 171–176.
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
38. D. Wang, A. Sakoda, M. Suzuki, Biological efficiency and
Pleurotus ostreatus in solid state fermentation, Process Bio-
nutritional value of Pleurotus ostreatus cultivated on spent
beer grain, Bioresour. Technol. 2001) 293–300. 54. V. Elisashvili, M. Penninckx, E. Kachlishvili, N. Tsiklauri,
39. Y.S. Cho, J.S. Kim, D.E. Crowley, B.G. Cho, Growth promo-
E. Metreveli, T. Kharziani, G. Kvesitadze, Lentinus edodes
tion of the edible fungus Pleurotus ostreatus by fluorescent
and Pleurotus species lignocellulolytic enzymes activity in
pseudomonads, FEMS Microbiol. Lett. (2003) 271–276.
submerged and solid-state fermentation of lignocellulosic
40. M.Q. Qu, Z.T. Xing, J.H. Chen, M.R. Li, D.Y. Men, N. Wang,
wastes of different composition, Bioresour. Technol. (in press).
W.M. Xie, Effect of heavy metal-containing substrates on
55. T. Watanabe, Y. Watanabe, K. Nakamura, Biodegradation
the yield and quality of Pleurotus eryngii fruiting bodies,
of wood in dual cultures of selected two fungi determined
Acta Edulis Fungi, 13 (2006) 57–60.
by chopstick method, J. Biosci. Bioeng. 95 (2003) 623–626. 41. N.L. Poyedinok, A.S. Buchalo, A.M. Negriyko, J.V. Potem-
56. Y. Chi, A. Hatakka, P. Maijala, Can co-culturing of two white-
kina, O.B. Mykchaylova, The action of argon and helium-
-rot fungi increase lignin degradation and the production
-neon laser radiation on growth and fructification of culi-
of lignin-degrading enzymes?, Int. Biodeter. Biodegr. 59 (2007)
nary–medicinal mushrooms Pleurotus ostreatus (Jacq.:Fr.)
Kumm., Lentinus edodes (Berk.) Singer, and Hericium erina-ceus (Bull.:Fr.) Pers., Int. J. Med. Mush. 5 (2003) 293–299. 57. F.C. Yang, C.B. Liau, The influence of environmental con-
ditions on polysaccharide formation by Ganoderma lucidum42. S. Berne, J. Pohleven, I. Vidic, D. Drobne, J. [trus, P. Ma-
in submerged cultures, Process Biochem. 33 (1998) 547–553.
~ek, F. Pohleven, K. Sep~i}, Ostreolysin, a cytolitic proteinfrom Pleurotus ostreatus with a putative role in fructifica-
58. M.T. Friel, A.J. McLoughlin, Production of a liquid inocu-
tion of the mushroom, Proceedings of the Fifth International
lum spawn of Agaricus bisporus, Biotechnol. Lett. 22 (2000)
Conference on Mushroom Biology and Mushroom Products,
59. F.J. Márquez-Rocha, G.K. Guillén, J.E. Sánchez, R. Vázquez-
43. G. Nasim, S.H. Malik, R. Bajwa, M. Afzal, S.W. Mian, Ef-
-Duhalt, Growth characteristics of Pleurotus ostreatus in bio-
fect of three different culture media on mycelial growth of
reactors, Biotechnol. Tech. 13 (1999) 29–32.
oyster and chinese mushrooms, OnLine Journal of Biological60. J.Z. Wu, P.C.K. Cheung, K.H. Wong, N.L. Huang, Studies
Sciences, 1 (2001) 1130–1133.
on submerged fermentation of Pleurotus tuber-regium (Fr.)
44. G. Zervakis, A. Philippoussis, S. Ioannidou, P. Diamanto-
Singer-Part 1: Physical and chemical factors affecting the
poulou, Mycelium growth kinetics and optimal tempera-
rate of mycelial growth and bioconversion efficiency, Food
ture conditions for the cultivation of edible mushroom
species on lignocellulosic substrates, Folia Microbiol. 46 (2001)
61. S.W. Kim, H.J. Hwang, J.P. Park, Y.J. Cho, C.H. Song, J.W.
Yun, Mycelial growth and exo-biopolymer production by
45. A. Gregori, B. Pahor, F. Pohleven, M. Berovi~, A. Pivec, K.
submerged culture of various edible mushrooms under dif-
Ri`nar: Materiali per{oji mi`narodnoji specializovanoji nauko-
ferent media, Lett. Appl. Microbiol. 34 (2002) 56–61. vo-prakticnoji konferenciji Gribna industrija, Kiev, Ukraine (2006)
62. F.R. Rosado, S. Germano, E.R. Carbonero, S.M.G. da Costa,
M. Iacomini, C. Kemmelmeier, Biomass and exopolysaccha-
46. S. Yildiz, E.D. Gezer, Ü.C. Yildiz, A. Temiz, E. Dizman, Ef-
ride production in submerged cultures of Pleurotus ostrea-
fects of different substrate combinations on mycelial growth
toroseus Sing. and Pleurotus ostreatus ‘’florida’’ (Jack.: Fr.)
of Pleurotus ostreatus, Proceedings of the Fifth International Con-
Kummer, J. Basic Microbiol. 43 (2003) 230–237. ference on Mushroom Biology and Mushroom Products, Shang-
63. J.C. Wang, S.H. Hu, Z.C. Liang, C.J. Yeh, Optimization for
the production of water-soluble polysaccharide from Pleu-47. S.G. Villas-Bôas, E. Esposito, M.M. de Mendonça, Biocon-
rotus citrinopileatus in submerged culture and its antitumor
version of apple pomace into a nutritionally enriched sub-
effect, Appl. Microbiol. Biotechnol. 67 (2005) 759–766.
strate by Candida utilis and Pleurotus ostreatus, World J. Mi-64. R.M.M. Gern, E. Wisbeck, J.R. Rampinelli, J.L. Ninow, S.A. crobiol. Biotechnol. 19 (2003) 461–467.
Furlan, Alternative medium for production of Pleurotus os-48. A. Sánchez, F. Ysunza, M.J. Beltran-Garcia, M. Esqueda, Bio-
treatus biomass and potential antitumor polysaccharides,
degradation of viticulture wastes by Pleurotus: A source of
Bioresour. Technol. (in press).
microbial and human food and its potential use in animal
65. H. Hou, J. Zhou, J. Wang, C. Du, B. Yan, Enhancement of
feeding, J. Agric. Food Chem. 50 (2002) 2537–2542.
laccase production by Pleurotus ostreatus and its use for the
49. B. Ghibom, S. Minkyung, L. Seungyong, H. Seokhwan, Re-
decolorization of anthraquinone dye, Process Biochem. 39
sponse surface analysis of solid state growth of Pleurotusostreatus mycelia utilizing whey permeate, Biotechnol. Lett.66. K.K. Prasad, S.V. Mohan, R.S. Rao, B.R. Pati, P.N. Sarma,
Laccase production by Pleurotus ostreatus 1804: Optimiza-
50. V. Elisashvili, M. Penninckx, E. Kachlishvili, M. Asatiani,
tion of submerged culture conditions by Taguchi DOE me-
G. Kvesitadze, Use of Pleurotus dryinus for lignocellulolytic
thodology, Biochem. Eng. J. 24 (2005) 17–26.
enzymes production in submerged fermentation of man-
67. N. Mikiashvili, S. Wasser, E. Nevo, V. Elisashvili, Effects of
darin peels and tree leaves, Enzyme Microb. Technol. 38 (2006)
carbon and nitrogen sources on Pleurotus ostreatus lignino-
lytic enzyme activity, World J. Microbiol. Biotechnol. 22 (2006)
51. G.V. Reddy, P. Ravindra Babu, P. Komaraiah, K.R.R.M. Roy,
I.L. Kothari, Utilization of banana waste for the produc-
68. S. Rodríguez, M. Fernández, R.C. Bermúdez, H. Morris, N.
tion of lignolytic and cellulolytic enzymes by solid sub-
García, Growth of Pleurotus ostreatus on the wastewater of
strate fermentation using two Pleurotus species (P. ostreatus
a mushroom farm, 4th International Conference on Mushroom
and P. sajor-caju), Process Biochem. 38 (2003) 1457–1462. Biology and Mushroom Products, Cuernavaca, Mexico (2002). 52. M. Staji}, L. Persky, D. Friesem, Y. Hadar, S.P. Wasser, E. 69. G. Aggelis, D. Iconomou, M. Christou, D. Bokas, S. Kot-
Nevo, J. Vukojevi}, Effect of different carbon and nitrogen
zailias, G. Christou, V. Tsagou, S. Papanikolaou, Phenolic
sources on laccase and peroxidases production by selected
removal in a model olive oil mill wastewater using Pleu-Pleurotus species, Enzyme Microb. Technol. 38 (2006) 65–73. rotus ostreatus in bioreactor cultures and biological evalua-
53. A. Mishra, S. Kumar, Cyanobacterial biomass as N-supple-
tion of the process, Water Res. 37 (2003) 3897–3904.
ment to agro-waste for hyper-production of laccase from
70. N. Jose, K.K. Janardhanan, Antioxidant and antitumour ac-
tivity of Pleurotus florida, Curr. Sci. 79 (2000) 941–943.
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
71. N. Jose, T.A. Ajith, K.K. Jananrdhanan, Antioxidant, anti-
87. M. Zhang, P.C. Cheung, L. Zhang, Evaluation of mushroom
-inflammatory, and antitumor activities of culinary-medic-
dietary fiber (nonstarch polysaccharides) from sclerotia of
inal mushroom Pleurotus pulmonarius (Fr.) Quel. (Agarico-Pleurotus tuber-regium (Fries) singer as a potential antitu-
mycetideae), Int. J. Med. Mush. 4 (2002) 59–66.
mor agent, J. Agric. Food Chem. 49 (2001) 5059–5062. 72. I.G. Meerovich, M. Yang, P. Jiang, R.M. Hoffman, V.P. Gera-
88. M. Zhang, L. Zhang, P.C.K. Cheung, V.E.C. Ooi, Molecular
simenya, A.E. Orlov, A.P. Savitsky, V.O. Popov, Study of
weight and anti-tumor activity of the water-soluble poly-
action of cyclophosphamide and extract of mycelium of Ple-
saccharides isolated by hot water and ultrasonic treatment
urotus ostreatus in vivo on mice, bearing melanoma B16-F0-
from the sclerotia and mycelia of Pleurotus tuber-regium, Car-
-GFP, Proceedings of the SPIE, Vol. 5704, Genetically Engine-bohydr. Polym. 56 (2004) 123–128. ered and Optical Probes for Biomedical Applications III, San Hose,
89. S.M. Wong, K.K. Wong, L.C.M. Chiu, P.C.K. Cheung, Non-
California, USA (2005) pp. 214–221.
-starch polysaccharides from different developmental sta-
73. Y.H. Gu, G. Sivam, Cytotoxic effect of oyster mushroom
ges of Pleurotus tuber-regium inhibited the growth of hu-
Pleurotus ostreatus on human androgen-independent pros-
man acute promyelocytic leukemia HL-60 cells by
tate cancer PC-3 cells, J. Med. Food. 9 (2006) 196–204.
cell-cycle arrest and/or apoptotic induction, Carbohydr.74. S.P. Wasser, Medicinal mushrooms as a source of antitu-
mor and immunomodulating polysaccharides, Appl. Micro-90. M. Zhang, L. Zhang, P.C. Cheung, Molecular mass and
biol. Biotechnol. 60 (2002) 258–274.
chain conformation of carboxymethylated derivatives of
75. M. Zhang, S.W. Cui, P.C.K. Cheung, Q. Wang, Antitumor
beta-glucan from sclerotia of Pleurotus tuber-regium, Biopo-
polysaccharides from mushrooms: a review on their isola-
lymers, 68 (2003) 150–159.
tion process, structural characteristics and antitumor activ-
91. M.E.I. Zhang, P.C.K. Cheung, L. Zhang, C.M. Chiu, V.E.C.
ity, Trends Food Sci. Technol. 18 (2007) 4–19.
Ooi, Carboxymethylated b-glucans from mushroom scle-
76. P.C. Cheung, M.Y. Lee, Fractionation and characterization
rotium of Pleurotus tuber-regium as novel water-soluble anti-
of mushroom dietary fiber (nonstarch polysaccharides) as
-tumor agent, Carbohydr. Polym. 57 (2004) 319–325.
potential nutraceuticals from sclerotia of Pleurotus tuber-re-92. Y. Tao, L. Zhang, P.C. Cheung, Physicochemical properties
gium (Fries) singer, J. Agric. Food Chem. 48 (2000) 3148–
and antitumor activities of water-soluble native and sul-
fated hyperbranched mushroom polysaccharides, Carbo-77. D. Chenghua, Y. Xiangliang, G. Xiaoman, W. Yan, Z. Jing-
hydr. Res. 341 (2006) 2261–2269.
yan, X. Huibi, A beta-d-glucan from the sclerotia of Pleu-93. M. Zhang, P.C.K. Cheung, L.C.M. Chiu, E.Y.L. Wong,
rotus tuber-regium (Fr.) Sing, Carbohydr. Res. 328 (2000) 629–
V.E.C. Ooi, Cell-cycle arrest and apoptosis induction in
human breast carcinoma MCF-7 cells by carboxymethyla-
78. L. Zhang, M. Zhang, J. Dong, J. Guo, Y. Song, P.C.K. Che-
ted [beta]-glucan from the mushroom sclerotia of Pleurotus
ung, Chemical structure and chain conformation of the wa-
tuber-regium, Carbohydr. Polym. 66, (2006) 455–462.
ter-insoluble glucan isolated from Pleurotus tuber-regium,
94. I. Lavi, D. Friesem, S. Geresh, Y. Hadar, B. Schwartz, An
Biopolymers, 59 (2001) 457–464.
aqueous polysaccharide extract from the edible mushroom
79. F.R. Rosado, E.R. Carbonero, C. Kemmelmeier, C.A. Tis-
Pleurotus ostreatus induces anti-proliferative and pro-apop-
cher, P.A.J. Gorin, M. Iacomini, A partially 3-O-methylated
totic effects on HT-29 colon cancer cells, Cancer Lett. 244
(1®4)-linked a-D-galactan and a-D-mannan from Pleuro-tus ostreatoroseus Sing, FEMS Microbiol. Lett. 212 (2002) 261–
95. H. Wang, J. Gao, T.B. Ng, A new lectin with highly potent
antihepatoma and antisarcoma activities from the oyster
80. F.R. Rosado, E.R. Carbonero, R.F. Claudino, C.A. Tischer,
mushroom Pleurotus ostreatus, Biochem. Biophys. Res. Com-
C. Kemmelmeier, M. Iacomini, The presence of partially
3-O-methylated mannogalactan from the fruit bodies of
96. R.G. Mahajan, S.I. Patil, D.R.K. Mohan, P. Shastry, Pleuro-
edible basidiomycetes Pleurotus ostreatus ‘florida’ Berk. tus eous mushroom lectin (PEL) with mixed carbohydrate
and Pleurotus ostreatoroseus Sing, FEMS Microbiol. Lett. 221
inhibition and antiproliferative activity on tumor cell lines,
J. Biochem. Mol. Biol. Biophys. 6 (2002) 341–345. 81. M. Zhang, L. Zhang, P.C. Cheung, J. Dong, Fractionation
97. P.H. Ngai, T.B. Ng, A ribonuclease with antimicrobial, anti-
and characterization of a polysaccharide from the sclerotia
mitogenic and antiproliferative activities from the edible
of Pleurotus tuber-regium by preparative size-exclusion chro-
mushroom Pleurotus sajor-caju, Peptides, 25 (2004) 11–17.
matography, J. Biochem. Biophys. Methods, 56 (2003) 281–
98. L. Xia, K.T. Chu, T.B. Ng, A low-molecular mass ribonu-
clease from the brown oyster mushroom, J. Pept. Res. 6682. M. Pramanik, S. Mondal, I. Chakraborty, D. Rout, S.S. Is-
lam, Structural investigation of a polysaccharide (Fr. II)
99. P. Ngai, T. Ng, A hemolysin from the mushroom Pleurotus
isolated from the aqueous extract of an edible mushroom,
eryngii, Appl. Microbiol. Biotechnol. 72 (2006) 1185–1191. Pleurotus sajor-caju, Carbohydr. Res. 340 (2005) 629–636. 100. I. Sarangi, D. Ghosh, S.K. Bhutia, S.K. Mallick, T.K. Maiti,
83. D. Rout, S. Mondal, I. Chakraborty, M. Pramanik, S.S. Is-
Anti-tumor and immunomodulating effects of Pleurotus
lam, Chemical analysis of a new (1®3)-, (1®6)-branched
ostreatus mycelia-derived proteoglycans, Int. Immunophar-
glucan from an edible mushroom, Pleurotus florida,
Carbohydr. Res. 340 (2005) 2533–2539. 101. V. Shlyakhovenko, V. Kosak, S. Olishevsky, Application of
84. D. Rout, S. Mondal, I. Chakraborty, S.S. Islam, The struc-
DNA from mushroom Pleurotus ostreatus for cancer bio-
ture of a polysaccharide from Fraction-II of an edible mush-
therapy: A pilot study, Experim. Oncol. 28 (2006) 132–135.
room, Pleurotus florida, Carbohydr. Res. 341 (2006) 995–1002. 102. D. Kamilya, D. Ghosh, S. Bandyopadhyay, B.C. Mal, T.K. 85. E.R. Carbonero, A.H.P. Gracher, F.R. Smiderle, F.R. Rosado,
Maiti, In vitro effects of bovine lactoferrin, mushroom glu-
G.L. Sassaki, P.A.J. Gorin, M. Lacomini, A b-glucan from the
can and Abrus agglutinin on Indian major carp, catla
fruit bodies of edible mushrooms Pleurotus eryngii and Ple-
(Catla catla) head kidney leukocytes, Aquaculture, 253urotus ostreatoroseus, Carbohydr. Polym. 66 (2006) 252–257. 86. Y. Tao, L. Zhang, Determination of molecular size and shape
103. J.C. Ho, S.C. Sze, W.Z. Shen, W.K. Liu, Mitogenic activity
of hyperbranched polysaccharide in solution, Biopolymers,
of edible mushroom lectins, Biochim. Biophys. Acta, 1671
A. GREGORI et al.: Cultivation of Pleurotus spp., Food Technol. Biotechnol. 45 (3) 236–247 (2007)
104. J.H. Yang, H.C. Lin, J.L. Mau, Antioxidant properties of
119. V. Nosál’ová, P. Bobek, S. Cerna, S. Galbavy, S. Stvrtina,
several commercial mushrooms, Food Chem. 77 (2002) 229–
Effects of pleuran (beta-glucan isolated from Pleurotusostreatus) on experimental colitis in rats, Physiol. Res. 50105. M. Filipic, A. Umek, A. Mlinaric, Screening of Basidiomy-
cete mushroom extracts for antigenotoxic and bio-antimu-
120. P. Bobek, V. Nosál’ová, S. Cerná, Effect of pleuran (b-glu-
tagenic activity, Die Pharmazie, 57 (2002) 416–420.
can from Pleurotus ostreatus) in diet or drinking fluid on
106. K.M. El Bohi, L. Sabik, K. Muzandu, Z. Shaban, M. Soli-
colitis in rats, Nahrung/Food, 45 (2001) 360–363.
man, M. Ishizuka, A. Kazusaka, S. Fujita, Antigenotoxic
121. M. Sano, K. Yoshino, T. Matsuzawa, T. Ikekawa, Inhibi-
effect of Pleurotus cornucopiae extracts on the mutagenesis
tory effects of edible higher basidiomycetes mushroom ex-
of Salmonella typhimurium TA98 elicited by benzo[a]pyrene
tracts on mouse type IV allergy, Int. J. Med. Mush. 4 (2002)
and oxidative DNA lesions in V79 hamster lung cells, Jpn.J. Vet. Res. 52 (2005) 163–172. 122. N. Gunde-Cimerman, A. Plemenitas, Hyporcholesterolemic
107. K. Taira, Y. Miyashita, K. Okamoto, S. Arimoto, E. Takaha-
activity of the genus Pleurotus (Jacq.: Fr.) P. Kumm. (Aga-
shi, T. Negishi, Novel antimutagenic factors derived from
ricales s. l., Basidiomycetes), Int. J. Med. Mush. 3 (2001) 395–
the edible mushroom Agrocybe cylindracea, Mutat. Res. 586123. S. Hossain, M. Hashimoto, E.K. Choudhury, N. Alam, S. 108. Y.I. Shi, A.E. James, I.F.F. Benzie, J.A. Buswell, Mushroom-
Hussain, M. Hasan, S.K. Choudhury, I. Mahmud, Dietary
-derived preparation in the prevention of H2O2-induced
mushroom (Pleurotus ostreatus) ameliorates atherogenic li-
oxidative damage to cellular DNA, Teratogen. Carcin. Mut.
pid in hypercholesterolaemic rats, Clin. Exp. Pharmacol.Physiol. 30 (2003) 470–475. 109. M. Elmastas, O. Isildak, I. Turkekul, N. Temur, Determina-
124. S.H. Hu, J.C. Wang, J.L. Lien, E.T. Liaw, M.Y. Lee, Anti-
tion of antioxidant activity and antioxidant compounds in
hyperglycemic effect of polysaccharide from fermented
wild edible mushrooms, J. Food Compos. Anal. 20 (2007)
broth of Pleurotus citrinopileatus, Appl. Microbiol. Biotechnol.110. N.J. Dubost, B. Ou, R.B. Beelman, Quantification of poly-
125. S.Y. Hagiwara, M. Takahashi, Y. Shen, S. Kaihou, T. Tomi-
phenols and ergothioneine in cultivated mushrooms and
yama, M. Yazawa, Y. Tamai, Y. Sin, A. Kazusaka, M. Tera-
correlation to total antioxidant capacity, Food Chem. (in
zawa, A phytochemical in the edible Tamogi-take mush-
room (Pleurotus cornucopiae), D-mannitol, inhibits ACE ac-
111. Y.L. Lee, G.W. Huang, Z.C. Liang, J.L. Mau, Antioxidant
tivity and lowers the blood pressure of spontaneously hy-
properties of three extracts from Pleurotus citrinopileatus,
pertensive rats, Biosci. Biotechnol. Biochem. 69 (2005) 1603–
Lebensm. Wiss. Technol. 40 (2007) 823–833. 112. S.H. Lo, Quality evaluation of Agaricus bisporus, Pleurotus126. V.P. Gerasimenya, O.V. Efremenkova, O.V. Kamzolkina TA. eryngii, Pleurotus ferulae and Pleurotus ostreatus and their
Bogush, I.V. Tolstych, V.A. Zenkova, Antimicrobial and
antioxidant properties during postharvest storage, MSc
antitoxical action of edible and medicinal mushroom Pleu-Thesis, National Chung-Hsing University, Taichung, Tai-
rotus ostreatus (Jacq.: Fr.) Kumm. Extracts, Int. J. Med. Mush.113. S.H. Hu, Z.C. Liang, Y.C. Chia, J.L. Lien, K.S. Chen, M.Y. 127. K. Okamoto, S. Narayama, A. Katsuo, I. Shigematsu, H.
Lee, J.C. Wang, Antihyperlipidemic and antioxidant ef-
Yanase, Biosynthesis of p-anisaldehyde by the white-rot
fects of extracts from Pleurotus citrinopileatus, J. Agric. Food
basidiomycete Pleurotus ostreatus, J. Biosci. Bioeng. 93114. T. Jayakumar, E. Ramesh, P. Geraldine, Antioxidant activ-
128. K. Periasamy, Novel antibacterial compounds obtained from
ity of the oyster mushroom, Pleurotus ostreatus, on CCl(4)-
some edible mushrooms, Int. J. Med. Mush. 7 (2005) 443–
-induced liver injury in rats, Food Chem. Toxicol. 44 (2006)
129. H. Wang, T.B. Ng, Eryngin, a novel antifungal peptide
115. T. Jayakumar, P.A. Thomas, P. Geraldine, Protective effect
from fruiting bodies of the edible mushroom Pleurotus
of an extract of the oyster mushroom, Pleurotus ostreatus,
eryngii, Peptides, 25 (2004) 1–5.
on antioxidants of major organs of aged rats, Exp. Ge-130. C.R. Brandt, F. Piraino, Mushroom antivirals, Recent Res.Dev. Antimicrob. Agents Chemother. 4 (2000) 11–26. 116. P. Bobek, S. Galbavy, Effect of pleuran (beta-glucan from
131. J. Wang, H.X. Wang, T.B. Ng, A peptide with HIV-1 re-
Pleurotus ostreatus) on the antioxidant status of the organ-
verse transcriptase inhibitory activity from the medicinal
ism and on dimethylhydrazine-induced precancerous le-
mushroom Russula paludosa, Peptides, 28 (2007) 560–565.
sions in rat colon, Brit. J. Biomed. Sci. 58 (2001) 164–168. 132. H.X. Wang, T.B. Ng, Isolation of a novel ubiquitin-like
117. L. Li, T.B. Ng, M. Song, F. Yuan, Z.K. Liu, C.L. Wang, Y.
protein from Pleurotus ostreatus mushroom with anti-hu-
Jiang, M. Fu, F. Liu, A polysaccharide–peptide complex
man immunodeficiency virus, translation-inhibitory, and
from abalone mushroom (Pleurotus abalonus) fruiting bod-
ribonuclease activities, Biochem. Biophys. Res. Commun. 276
ies increases activities and gene expression of antioxidant
enzymes and reduces lipid peroxidation in senescence-ac-
133. M. Zhang, L. Zhang, Y. Wang, P.C. Cheung, Chain confor-
celerated mice, Appl. Microbiol. Biotechnol. 75 (2007) 863–
mation of sulfated derivatives of beta-glucan from sclero-
tia of Pleurotus tuber-regium, Carbohydr. Res. 338 (2003)
118. N. Jose, T.A. Ajith, K.K. Janardhanan, Methanol extract of
the oyster mushroom, Pleurotus florida, inhibits inflamma-
134. M. Zhang, P.C. Cheung, V.E. Ooi, L. Zhang, Evaluation of
tion and platelet aggregation, Phytother. Res. 18 (2004) 43–
sulfated fungal beta-glucans from the sclerotium of Pleu-rotus tuber-regium as a potential water-soluble anti-viralagent, Carbohydr. Res. 339 (2004) 2297–2301.
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INSTRUCTION PRESENTED AND APPROVED: DECEMBER 7, 2012 INSTRUCTION Course Title: Psychopharmacology and Substance Abuse Change course title to reflect current terminology used in the field of substance abuse. If this is a change, what is being changed? A prerequisite changed was noted after the meeting. The box has been checked to reflect the Textbook/Reviewed Competencies-no changes