In the present study, a phylogenetic analysis was undertaken based on the internal transcribed spacer (ITS) rDNA and partial β-tubulin gene sequence of the Ganoderma species. The size of the ITS rDNA regions from different Ganoderma species varied from 625 to 673 bp, and those of the partial β-tubulin gene sequence were 419 bp. Based on the results, a phylogenetic tree was prepared which revealed that Korean Ganoderma lucidum strains belong in a single group along with a G. lucidum strain from Bangladesh.

Apple pomace is a by-product from the apple processing industry and has the potential to support the growth of microorganisms. In this study, the effect of apple pomace on the growth rate of Pleurotus ostreatus mycelium was investigated. The mycelial growth dramatically increased by 34.5, 20 and 26% in solid culture, liquid culture, and solid-state fermentation, respectively, by adding 2.5% apple pomace. However, the growth of P. ostreatus mycelia was slightly inhibited by adding 5 or 10% compared to 2.5% apple pomace. Our findings reveal that apple pomace utilization can become a model for the valuable addition of similar wastes, and for the development of a solid-state fermenter.

Ganoderma lucidum has long been used as a potent medicinal plant. In addition, recent studies showed that G. lucidum is used to prevent or treat various human diseases such as allergy, hepatopathy, hypertension, cancer and diabetes. In this study showed that ethanol extract from G. lucidum have potential inhibitory effects of glycerol 3-phosphat acyltransferase (GPAT) activity and increase of glucose uptake on skeletal muscle cells. Inhibition of GPAT, which catalyze the first step in de novo TAG synthesis, has been proposed as one of the drug targets for insulin resistance and type-2 diabetes. G. lucidum extract inhibited GPAT activity. Bioassay-guided fractionation and isolation of bio-active substances from ethanol extracts of G. lucidum were carried out by using chromatographic techniques and in vitro GPAT enzyme assay. One of bioactive molecules, ergosterol peroxide, was isolated and identified by physical and spectral properties. In this study showed that ethanol extract from G. lucidum and ergosterol peroxide have potential anti- diabetes effects through the increase of glucose uptake. This was as sociated with increased activity AMP-activated protein kinase(AMPK). AMPK is another regulatory protein in the glucose uptake pathway and energy metabolism. The result was that the increase of glucose uptake by G. lucidum extract might be mediated by AMPK.

The effects of Ganoderma lucidum on glucose uptake was studied in L6 rat skeletal muscle cells. Glucose uptake in muscle cell was increased about 6-fold compared to control by mushroom extract treatment. This increasing effect to the glucose uptake was observed in muscle cells cultured with or without insulin. The levels of phosphor-acetyl CoA carboxylase were upregulated by G. lucidum extract treatment in insulinstimulated and basal culture conditions. However, G. lucidum extract did not affect protein kinaseB/Akt(Akt) level. Furthermore, the expression of phosphor-AMPactivated protein kinase(AMPK) was also up-regulated. AMPK is another regulatory protein in the glucose uptake pathway and energy metabolism. Thus, the treatment of G. lucidum extract in skeletal muscle cells increased the phosphorylation levels of AMPK and acetyl-CoA carboxylase, showing that the increase of glucose uptake by G. lucidum extract might be mediated via the activation of AMPK signaling pathway

Mushroom is the only microorganism cultivated as the crop, and Plerotus ostreatus is one of the most important edible mushrooms. Efficient production of edible mushrooms relies on the precise control of fruiting body development, and an identification of the molecular mechanism of fruiting body development has commercial and scientific importance. In order to identify the developmentally regulated genes during fruiting body development, cDNA libraries were constructed from eight developmental stages of the P. ostreatus. From these libraries, 11,761 expressed sequence tags (ESTs) were generated. Based on these results, we performed macroarray analysis using 1,528 unigene clones at three developmental stages of mycelium, fruiting body and basidiospores. Plasmids isolated from these clones were blotted on the nylon membrane. The isotope-labelled cDNA probes for hybridization of the northern blot were prepared from total RNAs isolated from three developmental stages of mushroom. The 33, 14, 10 unigenes were very highly expressed in mycelia, fruit body and basidiospores, respectively. To confirm expression pattern of these genes, RT-PCR was performed using the total RNA isolated from three developmental stages. Seven genes were successfully amplified in RT-PCR. The expression patterns of the genes were similar with that in macroarray. One of seven genes was identified as a 12kDa heat shock protein and its expression level was very highly at fruiting stage, but not detected at mycelium stage.