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Drugs dedicated to alleviate neurodegenerative diseases like Parkinson’s and Alzheimer’s have always been associated with debilitating side effects. Medicinal mushrooms which harness neuropharmacological compounds offer a potential possibility for protection against such diseases. Pleurotus giganteus (formerly known as Panus giganteus) has been consumed by the indigenous people in Peninsular Malaysia for many years. Domestication of this wild mushroom is gaining popularity but to our knowledge, medicinal properties reported for this culinary mushroom are minimal.
The fruiting bodies P. giganteus were analysed for its nutritional values. Cytotoxicity of the mushroom’s aqueous and ethanolic extracts towards PC12, a rat pheochromocytoma cell line was assessed by using 3-[4,5-dimethythiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) assay. Neurite outgrowth stimulation assay was carried out with nerve growth factor (NGF) as control. To elucidate signaling mechanisms involved by mushroom extract-induced neurite outgrowth, treatment of specific inhibitor for MEK/ERK and PI3K signalling pathway was carried out.
The fruiting bodies of P. giganteus were found to have high carbohydrate, dietary fibre, potassium, phenolic compounds and triterpenoids. Both aqueous and ethanolic extracts induced neurite outgrowth of PC12 cells in a dose- and time-dependant manner with no detectable cytotoxic effect. At day 3, 25μg/ml of aqueous extract and 15μg/ml of ethanolic extract showed the highest percentage of neurite-bearing cells, i.e. 31.7±1.1% and 33.3±0.9%; respectively. Inhibition treatment results suggested that MEK/ERK and PI3K/Akt are responsible for neurite outgrowth of PC12 cells stimulated by P. giganteus extract. The high potassium content (1345.7mg/100g) may be responsible for promoting neurite extension, too.
P. giganteus contains bioactive compounds that mimic NGF and are responsible for neurite stimulation. Hence, this mushroom may be developed as a nutraceutical for the mitigation of neurodegenerative diseases.
Neurodegenerative diseases are on the rise. The most common form of neurodegenerative disease is Alzheimer's disease, which causes thinking and memory to become seriously impaired due to neuronal loss in brain . The second most common neurodegenerative syndrome, Parkinson's disease is characterised by the classic symptoms of tremors, rigidity and gait impairment . Medications to alleviate these neurodegenerative diseases can only provide benefits for several years but are not effective as the diseases progress . Some undesired side effects associated with these drugs include hallucinations, dyskinesia, nausea and constipation [2,3]. In this regard, complementary and alternative medicine which is now gaining momentum may be a promising way for prevention and protection against such neurodegenerative diseases .
Mushrooms are largely consumed not only in Asian countries but across Western countries. Mushrooms are of considerable interest because of their organoleptic merit, medicinal properties and economic significance. We have documented the effects of an edible mushroom Hericium erinaceus (Bull.:Fr.) Pers. (also known as monkey’s head, lion’s mane, and yamabushitake) on neurite outgrowth and peripheral nerve regeneration both in vitro and in vivo[5-7]. More recently, the aqueous extracts of Lignosus rhinoceros (Cooke) Ryvarden (tiger’s milk mushroom) was reported to induce neurite outgrowth with or without the trigger of nerve growth factor (NGF) . The cocktail of bioactive compounds present in these mushroom extracts exhibits NGF-like properties and play important roles in the growth, differentiation and survival of neuronal cells [9-11].
Formerly known as Panus giganteus (Berk) Corner, Pleurotus giganteus (Berk.) Karunarathna & K.D. Hyde is a culinary mushroom that is gaining popularity for its organoleptic properties and commercial prospects. In fact, consumption of this used-to-be wild mushroom has long been a tradition in the indigenous villages in Peninsular Malaysia . A variety of P. giganteus from China is now being cultivated in Malaysia and the common commercial name in Malay language for P. giganteus is “Seri Pagi” (morning glory). In China, P. giganteus is widely referred as “Zhudugu” (swine’s stomach) . It is noteworthy to mention that the “Panus-PleurotusLentinus” complex has long existed and has resulted in the confusion of nomenclature and taxonomy of these three species. Briefly, Panus giganteus (Polyporaceae, Polyporales) is characterised by its unbranched skeletal hyphae that usually grow on buried woody substrates . While Pegler  has merged Panus as a subgenus within Lentinus, Corner , has grouped the genus Panus to species with skeletal hyphae and separated those species with ligative hyphae in Lentinus. Hence, Lentinus giganteus is regarded as synonym for Panus giganteus and Lentinus giganteus should be used if recommendation of Pegler is ever adopted [13,16]. However, Karunarathna and colleagues have revisited this issue and concluded that Panus/Lentinus giganteus should be unified and positioned in Pleurotus as supported by molecular evidences .
Cell cultures derived from nervous system tissue have proven to be powerful tools for elucidating cellular mechanisms of nervous system function . The effect of chemicals, drugs, natural products or even growth factors on neurite outgrowth can be quantified by enumerating the number of cells that bear neurites using in vitro cell line model . Neurite refers collectively to “axons and dendrites extended by primary cells growing in culture, or processes extended by neuronal cell lines, which are neither definitive axons, nor dendrites” [19,20]. Pheochromocytoma (PC12) cells, originated from a rat adrenal medullary tumour (pheochromocytoma) have been widely employed as a model of neuronal differentiation and neurite outgrowth . PC12 cells respond to NGF and when triggered, cease proliferation, extend neurites, and become electrically excitable .
There is, however, minimal information on the medicinal properties of P. giganteus. The aqueous and ethanolic extracts of P. giganteus have shown antioxidant, genoprotection (unpublished data) and liver protection properties . To our knowledge, there are no reports on the nutritional composition of P. giganteus and its benefits on neurite outgrowth stimulation, if any. In the present study, aqueous and ethanolic extracts of P. giganteus fruiting bodies were investigated for their effects in neurite outgrowth of rat pheochromocytoma (PC12) cells. Prior to this, the cytotoxicity of the extracts was determined by using [3-[4,5-dimethythiazol-2-yl]-2,5-diphenyltetrazolium bromide] (MTT) assay. The hypothesis that MEK/ERK and PI3K/Akt are required for the neuronal differentiation and neurite outgrowth of PC12 cells was also tested using specific inhibitors.
The fruiting bodies of P. giganteus were obtained from Nas Agro Farm, Sepang, Selangor, Malaysia. Rat pheochromocytoma (PC-12) cell line was purchased from American Type Culture Collection (ATCC; Rockville, MD, USA; Catalogue Number: CRL-1721.1TM). [3-[4,5-dimethythiazol-2-yl]-2,5-diphenyltetrazolium bromide] (MTT), phosphate buffered saline (PBS), dimethyl sulfoxide (DMSO), F-12K medium (Kaighn’s Modification of Ham’sF-12 Medium), NGF-7S from murine submaxillary gland, MEK inhibitor (U0126, PD98059), and PI3K inhibitor (LY294002) were obtained from Sigma Co. (St. Louis, MO, USA). Fetal bovine serum (FBS) and horse serum (HS) were purchased from PAA Laboratories (Cölbe, Germany).
Pleurotus giganteus (KUM61102) was maintained on potato dextrose agar (PDA) at 4 - 10°C and regularly subcultured. The substrate formulation for the cultivation of P. giganteus is similar to that for oyster mushroom cultivation, i.e. 89 - 94% (w/w) rubber wood sawdust, 5 - 10% (w/w) rice bran and 1% (w/w) calcium carbonate. Polypropylene bags are used for substrate bagging and the moisture content in the substrate was kept at 60% - 65%. The temperature for mycelia growth, spawn run, and fruiting body formation is 26 - 32°C. Relative humidity of 70% and 80 - 90% during mycelia growth and fruiting; respectively, should be maintained. Direct illumination should be avoided as it has been reported to inhibit the fruiting body formation. A 20-day cycle after complete colonization of the artificial log is needed for each harvest and about four harvests (a total yield of 280g) can be obtained from each bag of 900g (Nas Agro Farm, personal communication).
The PC12 cells (adherent variant, PC-12Adh) from ATCC were maintained in F-12K medium (Sigma) supplemented with 2.5% (v/v) heat-inactivated fetal bovine serum (PAA) and 15% (v/v) horse serum (PAA) with final pH 6.8 - 7.2. All incubations were performed at 37°C in a humidified environment of 5% CO2 and 95% air. The cells were maintained in the logarithmic phase of growth and were subcultured at 2–3day intervals. For storage, the cells were frozen at −70°C liquid nitrogen in complete medium supplemented with 5% (v/v) dimethyl sulfoxide (DMSO) (Sigma) as a cryoprotectant.
The fresh fruiting bodies were sliced, weighed and freeze-dried (Christ, Germany) for 1–2days. The freeze-dried fruiting bodies were then ground using a blender. The resulting dried powder was weighed and kept in 4 - 8°C. Aqueous extraction method was according to Eik et al. . Briefly, the freeze dried powder was soaked in distilled water (1:20 ratio, w/v) and was left overnight at room temperature and 200rpm in a shaker. The mixture was double boiled in water bath for 30min and filtered (Whatman Grade 4) after cooling. The resulting aqueous extract was freeze-dried and kept at −40°C prior to use. For ethanol extraction, the freeze dried powder was soaked in 95% ethanol at room temperature for three days and the process was repeated three times. The ethanol solvent was evaporated using a rotary evaporator (Eyela N-1000, USA) to give a brownish viscous extract.
Fifty grams sample of P. giganteus fruiting bodies was sent to Consolidated Laboratory (M) Sdn. Bhd. for nutritional analysis.
Cell viability and proliferation was determined by MTT assay . Approximately 12,000 cells per well were seeded on a 96-well plate and incubated at 37°C overnight in a humidified environment of 5% CO2 and 95% air. Fresh medium were then replaced and the cells were exposed to 0 to 1000μg/ml of aqueous or ethanolic extract of P. giganteus for 48 hours. Subsequently, 20μl of sterilized MTT (5mg/ml) in phosphate buffered saline (PBS) buffer (pH 7.4) was spiked into each well and incubated at 37°C for 4 hours. The supernatant was then carefully removed, and 200μl of dimethyl sulfoxide (DMSO) was added into each well to dissolve the MTT formazan (blue colour) at the bottom of the wells. After 15min, the absorbance at 540nm with 690nm as background absorbance was measured with an ELISA microplate reader (Sunrise, Tecan, Austria). The complete growth medium was the blank, and cells incubated in medium only without mushroom extracts were denoted as positive control.
Neurite outgrowth stimulation assay was according to Eik et al.  with some modifications. The cells were seeded in a 6-well plate at an initial density of 5,000 cells per well in 2ml complete growth medium with different concentrations of aqueous and ethanolic mushroom extracts. For freeze dried aqueous extract, a stock solution of 10mg/ml was prepared freshly each time prior to assay. The stock solution was then diluted five times in sterile distilled water to final concentrations ranging from 5–100μg/ml (w/v). For ethanolic extract, 10mg/ml of stock solution in DMSO was prepared freshly. The solution was also diluted five times with sterile distilled water. In positive control experiments, cells were induced to differentiate by the addition of 50ng/ml (w/v) NGF extracted from murine submaxillary gland (Sigma). Cells in complete growth medium only served as a negative control. All the cells were incubated for five days at 37°C, 95% air and 5% CO2 to observe any neuronal differentiation activity.
A cell was scored positive if it bears a thin neurite extension that was double or more the length of the cell body diameter . Ten fields per well were randomly examined under an inverted microscope (Nikon Eclipse TS100). The cells were photographed using a Nikon DS-Fi1 camera and processed with a Nikon’s Imaging Software, NIS-Elements D. The percentage of neurite- bearing cells were quantified by scoring the number of neurite-bearing cells over the total number of viable cells in 10 microscopic fields with average of randomly chosen 200 to 300 cells per well.
Stock solution (10mM) of MEK inhibitor (U0126, PD98059) and PI3K inhibitor (LY294002) were prepared in DMSO and stored in −20°C in the dark. Each inhibitor i.e. 10μM for U0126 , 10–50μM of LY294002 ; and 40μM for PD98059  was then prepared by diluting in medium just before use. PC12 cells were either incubated with or without the treatment of inhibitors for 1 hour. All the cells were then stimulated with 25μg/ml of P. giganteus aqueous extract for three days prior to scoring neurite bearing cells.
Results were expressed as the means±standard deviation (SD). Data comparison between groups was performed using one-way analysis of variance (ANOVA). P<0.05 was considered to be significant between groups by using Duncan's multiple range tests (DMRT).
The nutritional components of P. giganteus fruiting bodies are shown in Table Table1.1. Pleurotus giganteus contains 67.2g/100g of carbohydrate, 15.4g/100g of protein and 33.3g/100g of dietary fibre. It is rich in minerals like magnesium (67.64mg/100g) and potassium (1345.7mg/100g).
MTT assay was performed to determine the degree of cytotoxicity of P. giganteus extracts in PC12 cell. The cell viability and cell proliferation was denoted as 100% for the positive control i.e. cells in complete growth medium without mushroom extracts. It was shown that the growth of PC12 cell decreased with the increasing concentrations of the mushroom extracts. Figure Figure1a1a and the negative region of Figure 1b and 1c indicates that treatment with 10–200μg/ml of aqueous extract and 10μg/ml of ethanolic extract induced cell proliferation significantly (p<0.05) as compared to control after a 48h incubation. Upon challenge with a threshold dosage (500μg/ml for aqueous extract and 200μg/ml for ethanolic extract), the number of viable cells decreased significantly (p<0.05) to 13.9% and 37.1%, respectively. At a concentration of 1000μg/ml, the different extracts inhibited the cell proliferation to 75.65±5.8% for aqueous extract, and 85.67±5.3 for ethanolic extract. The IC50 which is the concentration at which 50% of cell growth inhibition occurs for aqueous extract and ethanolic extract were 806.39±48μg/ml and 309.46±46μg/ml, respectively. Hence, ethanolic extract is more toxic compared to aqueous extract, as the IC50 of ethanolic extract was 2.6-fold higher than that of aqueous extract.
All concentrations of mushroom extracts tested were non-cytotoxic to the cells, as determined by MTT assay. Aqueous extract of P. giganteus induced neurite outgrowth of PC12 cells in both a time- and dose-dependent manner (Figure (Figure2a).2a). On the second day, the percentage of neurite-bearing cells increased significantly (p<0.05) to 18.8% after treatment with 25μg/ml of aqueous extract when compared to time-matched negative control (9.5%). After stimulation with aqueous extract, the percentage of neurite-bearing cells significantly increased (p<0.05) until the effect reached a plateau after day 3. Therefore, day 3 was selected for further studies as the neurite scoring for all concentrations were the highest. Similarly, ethanolic extract induced neurite outgrowth of PC12 cells in a time- and dose-dependent manner and the number of neurite-bearing cells remained constant after day 3, as shown in Figure Figure22(b).
Figure Figure2c2c and 2d give the percentage of neurite-bearing cells for aqueous extract and ethanolic extract, respectively, on day 3. As shown in Figure Figure2c,2c, aqueous extract at 25μg/ml had a significant (p<0.05) effect (31.7±1.1%) in stimulating neuronal differentiation compared to NGF (28.3±0.4%). On day 3, 15μg/ml of ethanolic extract induced 33.3±0.9% of neurite-bearing cells (Figure (Figure2d).2d). There was no significant difference (p>0.05) in the percentage of neurite-bearing cells at 25μg/ml of aqueous extract and 15μg/ml of ethanolic extract. However, both the extracts performed better than NGF (p<0.05). It was obvious for ethanolic extract, that 50μg/ml, 75μg/ml and 100μg/ml did not significantly (p>0.05) trigger neuronal differentiation and neurite outgrowth of PC12 as compared to aqueous extract for the same concentrations. Figure Figure33 shows the morphology of PC12 cells with neurites at day-3 of treatment with 50ng/ml NGF (a), 25μg/ml of aqueous extract (b), and neither of them (c).
It was shown that neurite outgrowth induced by NGF and aqueous extract of P. giganteus was markedly inhibited (p<0.05) by MEK inhibitors U0126 and PD98059 (Figure (Figure4a4a and 4b). In fact, in PC12 cell treated with aqueous extract combined with either 10μM of U0126 or 40μM of PD98059, the decrease in the number of neuritic processes was significant (p<0.05). On the contrary, an inhibitor of PI3K/Akt pathway, LY294002, did not inhibit aqueous extract- and NGF-induced neurite outgrowth at the concentration of 10μM and 20μM (p>0.05). LY294002 at the concentration of 30μM started to cause inhibition effects on PC12 in a concentration-dependent manner. At 30μM of LY294002, the number of elongated PC12 cells with neurites doubled the cell diameter decreased significantly, by 49.6% and 63.5%, for NGF- and aqueous extract-treated cells; respectively (Figure (Figure4c).4c). At 50μM, all the cells pre-treated with the inhibitor showed no difference (p>0.05) to the negative controls, with differentiated cells bearing neurites ranging only from 3.2 – 5.3%. From this result, we proposed that aqueous extract induced neurite outgrowth on PC12 cells via the activation of ERK1/2 cascade and PI3K/AKt pathways.
There is a vast amount of nutritional studies of wild and cultivated mushrooms across the world. However, relatively little data exist in the literature on the nutrient content of Pleurotus giganteus. Herein, it was intended to compare only the highly appreciated and most cultivated culinary-medicinal mushrooms, for example the Pleurotus genus and Agaricus genus. Generally, mushrooms have high (19 – 35%) protein contents . In Brazil, it was reported that the fruiting bodies of Pleurotus ostreatus and Pleurotus sajor-caju presented protein content ranging from 13.1% to 18.4%, depending on the substrates used . The present study showed that the protein level of P. giganteus is 5.3-time lower than that of Agaricus bisporus (white button mushroom) with reference to a study from Portugal . On the other hand, the carbohydrate content in P. giganteus is 4-, 6-, 7.2-, 7.5-, 8-, 11-time higher than that of Lentinula edodes, shiitake (17.12g/100g), Flammulina velutipes, golden needle mushroom (10.57g/100g), Pleurotus ostreatus, oyster mushroom (9.30g/100g), Pleurotus eryngii, king oyster mushroom (8.95g/100g), Agaricus bisporus white button mushroom (8.25g/100g) (30), and Agaricus bisporus brown mushroom (5.98g/100g) . This suggested that carbohydrates (glucose, mannitol, trehalose, oligosaccharide groups, and reserved polysaccharide like glycogen) account for the prevailing component of P. giganteus fruiting body. Reports related to the nutritional evaluation of Pleurotus genus carried out by other researchers from different regions (Japan, India, Bangladesh, Turkey, Finland, and Italy) can be retrieved from [32-37], respectively. Nevertheless, the differences between the nutrient values may be attributed to the type of mushroom, strain of mushroom, environmental factors, and composition of growth media .
MTT assay is by far the most convenient colorimetric assay based on the metabolic activity of a viable cell [24,38]. Basically, only viable cell has the mitochondrial dehydrogenase system that can cleave the yellow MTT tetrazolium salt and yield MTT formazan which is blue in colour. Thus, the optical density of the amount of solubilised MTT formazan is quantitatively correlated to the percentage of cell viability. The present study showed that cytotoxic effect of P. giganteus aqueous and ethanolic extracts towards PC12 cells were concentration dependant. This is consistent with the finding by Cheung et al.  whereby viability of PC12 cells was dose-dependently decreased by increasing Ganoderma lucidum extracts.
On-going studies show that the aqueous extract of P. giganteus contains bioactive secondary metabolites like sterols and triterpenes (unpublished data). These compounds are reported to have neutrophic NGF-like properties and caused neurite outgrowth activity in PC12 cells . We have shown for the first time that P. giganteus extract can stimulate neurite outgrowth by using PC12 cell line model. It was shown that 25μg/ml of aqueous extract and 15μg/ml of ethanolic extract induced the highest percentage of neurite outgrowth in PC12 cells at day 3. The number of neurite bearing cells was significantly higher than that of NGF. The mushroom extracts may contain bioactive compounds either mimic NGF or trigger the production of NGF, hence resulting in neurite outgrowth. Further, the potassium level in P. giganteus was 1345.7mg/100g and according to Kalac , potassium level in fruiting bodies is between 20- and 40-fold higher than in the substrates used for mushroom cultivation. In the study by Cohen-Cory et al. , the cell number of Purkinje cells, the major efferent neurons of the brain cerebellum increased by 40% when treated with potassium. Besides, potassium alone or potassium coupled with NGF markedly increased the cell survival, cell differentiation and neurite outgrowth. In this study, the potassium present in P. giganteus extracts may be involved in the regulation of the morphological differentiation of PC12 cells by acting as a depolarising agent.
The present study extends recent findings that some mushroom extracts can have neuritogenesis effects. Prior studies by our group have shown that 0.2% (v/v) aqueous extract of freeze dried fruiting bodies from Hericium erinaceus caused maximal stimulation of neurite outgrowth (17.3% of neurite bearing cells and 88.2% increase compared to control) in NG108-15 cell line after 24 hours of incubation . Besides, freeze drying was found to be the best approach to preserve the bioactive compounds in mushroom as compared to oven-dried method . It had been reported that PC12 cells responded well to water extract of sclerotium of Lignosus rhinocerus (Cooke) Ryvarden . It was found that synergistic effect, i.e. 42.12% of neurite bearing PC12 cells was elicited when the cells were treated with 20μg/ml of water extract combined with 30ng/ml of NGF. Some other medicinal mushrooms that induced neurite outgrowth included Grifola frondosa (Maitake) , Tricholoma sp , Termitomyces albuminosus[45,46], Dictyophora indusiata, Tremella fuciformis, and Ganoderma lucidium (Lingzhi) .
The involvement of the MAPK/ERKs signaling pathway in neuronal differentiation by mushroom extracts has been reported. Neuroprotective and neuritogenesis effect of Ganoderma lucidium extracts on PC12 was stipulated to be mediated via the MAPK/ERK signalling pathway . Besides, lysophosphatidylethanolamine from Grifola frondosa induced activation of ERK1/2 of PC12 cells thus stimulated neurite outgrowth and inhibited serum withdrawal-induced apoptosis . Neurotrophins like NGF are mostly mediated by the Trk family of receptor tyrosine kinase, TrKA. However, discrepancy did occur in the case of Ganoderma lucidium extracts, whereby there was no direct involvement of TrkA . Similarly, α-Phenyl-N-tert-butylnitron was also found to induce neurite outgrowth in PC12 independent of TrkA . It is thus predicted, based on the ability of P. giganteus extract to stimulate neurite outgrowth of PC12 without NGF, that activation of TrKA receptor tyrosine kinase may not be necessary. According to Sweatt , the mitogen-activated protein kinase (MAP kinase, MAPK) cascade is a superfamily of signalling cascade and is a vital regulator of cell division and differentiation. Recently, MAPK was specified as the extracellular signal-regulated kinase (ERK) comprising ERK 1 and 2, or as ERK1/2. It has been demonstrated that ERK-cascade was necessary and sufficient enough for NGF-induced neuronal differentiation of PC12 cells. In the present study, upon inhibition by MEK-selective inhibitor U0126 and PD98059, the percentage of neurite outgrowth decreased significantly. This suggested that ERK1/2 phosphorylation was affected and this indirectly implied that activation of ERK1/2 is necessary for P. giganteus-mediated neuritogenesis. Inhibition of PI3K/Akt signalling by LY294002 also negatively affected neurite outgrowth of PC12. This finding suggested that neurite outgrowth potentiated by P. giganteus in PC12 cells is also regulated by PI3K/Akt signaling pathway. However, it was noted that PI3K/Akt inhibitor did not markedly affect the activities of ERK , therefore neurite extension of PC12 still could be observed at lower concentrations of LY294002. According to Naidu et al. , phospho-Akt and phospho-MAPK were expressed during neurodevelopment and nerve regeneration following sciatic nerve crush on rats. Collectively, these results demonstrated that P. giganteus-induced neurite extension is regulated at least by part between MEK/ERK and PI3K/Akt pathways. For the future work, confirmation by immunoblot analysis to detect the phosphorylation of TrKA, ERK, and Akt, is necessary.
To our knowledge, this is the first evidence on the effects of Pleurotus giganteus aqueous and ethanol extracts on neuronal differentiation and neurite outgrowth. The high potassium level in the fruiting bodies and the presence of bioactive compounds (mainly triterpenoids) could be responsible for the neuroactivity. Work is in progress to determine and identity the bioactive compound/s responsible for the activity. Our results suggested that neurite outgrowth stimulated by P. giganteus is mediated via the “cross-talk” between MEK/ERKs and PI3K/Akt pathways. However, further immunoblot analysis is required.
The authors declare that they have no competing interests.
CWP carried out the experiment, drafted the manuscript, and engaged in data acquisition and data interpretation. WLW carried out ethanol extraction, and preparation of samples for nutritional analysis. PD participated in the acquisition of funding and editing for manuscript. MN involved in the design of the study and manuscript editing. VS provided the grant, involved in coordinating and monitoring of research; and manuscript editing. All authors read and approved the final manuscript.
The pre-publication history for this paper can be accessed here:
The authors thank Mr Nabil Sanusi (Nas Agro Farm) and Mr Jeff Kong (Dong Foong Biotech), for providing fresh fruiting bodies of Pleurotus giganteus. The authors also thank University of Malaya for supporting funds RG158/11AFR, Postgraduate Research Grant (PV007/2012A), RG136/10AFR, 66-02-03-0074, and Ministry of Higher Education for High Impact Research (HIR) grant, F000002-21001.