scholarly journals Possibility of modernization of Ganoderma lucidum strains substrate

2005 ◽  
Vol 11 (2) ◽  
Author(s):  
P. Maszlavér ◽  
D. Kovácsné ◽  
K. Ferenc ◽  
E. Fehérvári-Póczik

Ganoderma lucidum (Reishi mushroom), the object of our experiments, is also known to contain medicinal compounds. This fungus has been used for many centuries as medicine in China. The fruiting body of the fungus contains carbohydrates, amino acids, little protein, fat, alkaloids, vitamins and minerals. Two groups of its substances are reported to be effective particularly. One of them is constituted by the polysaccharides, whose antitumor and immunostimulating effects are well demonstrated, and the other is constituted by the triterpenes. The latter include ganoderic acids, ganolucidic acids and lucideric acids. These acids have been reported to suppress liver hyperactivity (Lelley 1999). The experiment was carried out with 8 Reishi mushroom strains in 3 repetitions. Experiments were performed on 3 different substrates The spawn run period took approximately 2 weeks, the first fruiting bodies appeared on the 33rd day from inoculation, but the formation of the fruiting bodies took almost 70 days on the different substrates. Spawn run presented a diversified picture as influenced by the specific substrates. No spawn run was seen with any of the strains on the substrate composed of 100% wheat straw. Among the strains the fastest spawn run was produced by GA02 and GA06. The earliest start of spawn run was registered for substrate 1 after 1 week.

Author(s):  
Darija Cör ◽  
Tanja Botić ◽  
Andrej Gregori ◽  
Franc Pohleven ◽  
Željko Knez

It is known that the lingzhi mushroom Ganoderma lucidum (Fr.) Karst produces various, bioactive metabolites. The objective of this study was to evaluate the antioxidant activity and acetylcholinesterase inhibitory activity of various extracts obtained from G. lucidum fruiting body and primordium, which is the initial stage of the mushroom’s fruiting body. Classical extraction of G. lucidum fruiting bodies and primordia using different solvents (water, methanol, acetone, ethanol and hexane) at two temperatures (at 25 °C and at the boiling point of the solvent) was performed.The influence of a solvent on the extraction yields and afterwards on the activity of the extract was observed. The extracts are rich in phenols, polysaccharides and proteins. The highest yield of 23.30% was obtained after water extraction. The total phenolic content was between 9 mgGA/g and 74.36 mgGA/g for G. lucidum fruiting bodies extracts and from 11.16 mgGA/g to 103.32 mgGA/g for G. lucidum primordia extracts. The antioxidant activity using the DPPH* free radical scavenging method was from 0.48% to 23.66% and from 5.32% to 54.57% for fruiting bodies and primordia extracts, respectively.Assessment of acetylcholinesterase enzyme inhibition was carried out using a colorimetric method based on Ellman’s reaction. Acetylcholinesterase enzyme inhibition (AChE inhibition) by G. lucidum fruiting bodies extracts was between 18.1% and 32.5%. The highest AChE inhibitory activity of primordia extracts was 29.48%. This is the first report of G. lucidum primordia extracts and their biological activity.


Author(s):  
Shuai Zhou ◽  
Xiaoyu Zhang ◽  
Fuying Ma ◽  
Shangxian Xie ◽  
Chuanhong Tang ◽  
...  

To systemically understand the biosynthetic pathways of bioactive substances, including triterpenoids and polysaccharides, in Ganoderma lucidum, the correlation between substrate degradation, carbohydrate and triterpenoid metabolism during growth was analyzed by combining changes in metabolite content and changes in related enzyme expression in G. lucidum over 5 growth phases. Changes in low-polarity triterpenoid content were correlated with changes in glucose and mannitol content in fruiting bodies. Additionally, changes in medium-polarity triterpenoid content were correlated with changes in the lignocellulose content of the substrate and with the glucose, trehalose and mannitol contents of fruiting bodies. Weighted gene coexpression network analysis (WGCNA) indicated that changes in trehalose and polyol content were related to carbohydrate catabolism and polysaccharide synthesis. Changes in triterpenoid content were related to expression of the carbohydrate catabolic enzymes, laccase, cellulase, hemicellulase, and polysaccharide synthase and to the expression of several cytochrome P450 monooxygenases (CYPs). It was concluded that the products of cellulose and hemicellulose degradation participate in polyol, trehalose and polysaccharide synthesis during initial fruiting body formation. These carbohydrates accumulate in the early phase of fruiting body formation and are utilized when the fruiting bodies mature and a large number of spores are ejected. An increase in carbohydrate metabolism provides additional precursors for the synthesis of triterpenoids. Importance Most studies of G. lucidum have focused on its medicinal function and on the mechanism of its activity, whereas the physiological metabolism and synthesis of bioactive substances during the growth of this species have been less studied. Therefore, theoretical guidance for cultivation methods to increase the production of bioactive compounds remains lacking. This study integrated changes in the lignocellulose, carbohydrate and triterpenoid contents of G. lucidum with enzyme expression from transcriptomics data using WGCNA. The findings helped us better understand the connections between substrate utilization and the synthesis of polysaccharides and triterpenoids during the cultivation cycle of G. lucidum. The results of WGCNA suggest that the synthesis of triterpenoids can be enhanced not only through regulating the expression of enzymes in the triterpenoid pathway, but also through regulating carbohydrate metabolism and substrate degradation. This study provides a potential approach and identifies enzymes that can be targeted to regulate lignocellulose degradation and accelerate the accumulation of bioactive substances by regulating substrate degradation in G. lucidum.


1966 ◽  
Vol 8 (1) ◽  
pp. 61-72 ◽  
Author(s):  
Lorna A. Casselton ◽  
D. Lewis

Artificially selected diploids of Coprinus lagopus when mated in compatible combinations, either together or with haploids, produce dikaryotic mycelia which are typical of normal haploid-haploid dikaryons. In a diploid-haploid dikaryon, the diploid nucleus is not as stable as when alone in a monokaryon but it can persist through repeated sub-culturing into a fruiting body and eventually through meiosis into the basidiospores. In a diploid–diploid dikaryon either one or the other nucleus becomes haploid so that fruiting bodies with two diploid nuclei are never formed. This fact constitutes a restriction on diploidy in nature and a useful method of reducing diploids to the haploid state.Matings that might be considered to be incompatible at the B mating gene show a significant difference which is related to the number of B alleles common to the mating colonies. Matings with one B allele in common, e.g. B3B6+B2B3 produce fully compatible and normal dikaryons. Matings with two B alleles in common, e.g. B3B6+B3B6 have, at first while the diploid nuclei still persist, the appearance of an incompatible common B haploid heterokaryon. This indicates that the B incompatibility system is based not on a complementary action between different B alleles but on an oppositional action between the same alleles neutralizing the B gene product which is necessary for dikaryon formation.


2019 ◽  
Vol 20 (11) ◽  
pp. 2830 ◽  
Author(s):  
Li Meng ◽  
Xiaoran Bai ◽  
Shaoyan Zhang ◽  
Mengfei Zhang ◽  
Sen Zhou ◽  
...  

Ganoderic acids (GAs) are a type of highly oxygenated lanostane-type triterpenoids that are responsible for the pharmacological activities of Ganoderma lucidum. They have been investigated for their biological activities, including antibacterial, antiviral, antitumor, anti-HIV-1, antioxidation, and cholesterol reduction functions. Inducer supplementation is viewed as a promising technology for the production of GAs. This study found that supplementation with sodium acetate (4 mM) significantly increased the GAs content of fruiting bodies by 28.63% compared to the control. In order to explore the mechanism of ganoderic acid accumulation, the transcriptional responses of key GAs biosynthetic genes, including the acetyl coenzyme A synthase gene, and the expression levels of genes involved in calcineurin signaling and acetyl-CoA content have been analyzed. The results showed that the expression of three key GAs biosynthetic genes (hmgs, fps, and sqs) were significantly up-regulated. Analysis indicated that the acetate ion increased the expression of genes related to acetic acid assimilation and increased GAs biosynthesis, thereby resulting in the accumulation of GAs. Further investigation of the expression levels of genes involved in calcineurin signaling revealed that Na+ supplementation and the consequent exchange of Na+/Ca2+ induced GAs biosynthesis. Overall, this study indicates a feasible new approach of utilizing sodium acetate elicitation for the enhanced production of valuable GAs content in G. lucidum, and also provided the primary mechanism of GAs accumulation.


Plant Disease ◽  
2013 ◽  
Vol 97 (11) ◽  
pp. 1507-1507 ◽  
Author(s):  
W. H. Dong ◽  
Y. B. Bian

Coprinus comatus, the shaggy mane, is one of the most popular and widely cultivated edible mushrooms in China. Its young fruiting body has good nutritional and medicinal value as well as a special flavor. In July 2010, an unusual stipe rot symptom was observed in cultivation tunnels in Pingyin county of Shandong Province. The lower part of the stipe was infected and water soaked scab occurred. The scab then expanded, a few mycelia and pink spores emerged on the scab surface, and finally, the stipe decayed and the fruiting body became wilted. The pathogen was isolated from infected tissues of C. comatus and the colonies on CYM were whitish at first, then pink sorus emerged, later forming concentric rings of sporulation. Mycelia were floccose, colorless, slender, and septate. Conidiophores bore upright, nonbranched, and colorless sporogenous cells, and slightly rounded spores were borne on the top and aggregated in pink cephaloid. Conidia were obovoid or obpyriform. Almost all spores were two-celled and one septate, while one was nearly round and the other bore an apex (1). The size of spores ranged from 10 to 21 μm long and 5 to 7 μm wide, which was consistent with the characteristics of Trichothecium roseum (1). The species identification was confirmed by sequencing the ribosomal ITS sequences. The ribosomal ITS1-5.8S-ITS2 region was amplified from the isolated strain using primers ITS1 and ITS4. A BLAST search in GenBank revealed the highest similarity (99%) to T. roseum (JQ434580). Pathogenicity was tested on different parts of 20 fruiting bodies of C. comatus with or without the wound treatment. One inoculum was prepared by flooding the agar surface with sterilized double distilled water for spore suspension (6.5 × 103 conidia/ml), and the other was by 0.2 × 0.2 cm mycelial plugs without spore production on CYM at 25°C for 5 days. After 1 to 2 days, only inoculated stipes showed water soaked and slight decay on the injured surface of all 20 fruiting bodies, while control fruiting bodies remained healthy. The symptoms were similar to those observed in the cultivation tunnels. No symptom was observed on the pileus, either with or without wound treatment. Pathogens reisolated from the inoculated stipes were confirmed to be T. roseum based on morphological characteristics. Because T. roseum is generally regarded as a postharvest disease of fruits and vegetables such as apple, pear, and muskmelon (2), apples and pears were inoculated with this fungus as well using the same methods. The parts inoculated were sunken, wettish, and decayed with brown stain at 25°C and 90% relative humidity after 5 days. Thus, it was confirmed that the T. roseum from the C. comatus stipe canker could infect the fruits of apple and pear. To our knowledge, this is the first report that T. roseum can cause disease on agaric. References: (1) G. Dal Bello. Australas. Plant Dis. Notes 3:103, 2008. (2) J.-H. Kwon et al. Plant Pathol. J. 26:296, 2010.


Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4484
Author(s):  
Nooruddin-bin Sadiq ◽  
Da-Hye Ryu ◽  
Jwa-Yeong Cho ◽  
A-Hyeon Lee ◽  
Dae-Geun Song ◽  
...  

Ganoderma lucidum extract is a potent traditional remedy for curing various ailments. Drying is the most important postharvest step during the processing of Ganoderma lucidum. The drying process mainly involves heat (36 h at 60 °C) and freeze-drying (36 h at −80 °C). We investigated the effects of different postharvest drying protocols on the metabolites profiling of Ganoderma lucidum using GC-MS, followed by an investigation of the anti-neuroinflammatory potential in LPS-treated BV2 microglial cells. A total of 109 primary metabolites were detected from heat and freeze-dried samples. Primary metabolite profiling showed higher levels of amino acids (17.4%) and monosaccharides (8.8%) in the heat-dried extracts, whereas high levels of organic acids (64.1%) were present in the freeze-dried samples. The enzymatic activity, such as ATP-citrate synthase, pyruvate kinase, glyceraldehyde-3-phosphatase dehydrogenase, glutamine synthase, fructose-bisphosphate aldolase, and D-3-phosphoglycerate dehydrogenase, related to the reverse tricarboxylic acid cycle were significantly high in the heat-dried samples. We also observed a decreased phosphorylation level of the MAP kinase (Erk1/2, p38, and JNK) and NF-κB subunit p65 in the heat-dried samples of the BV2 microglia cells. The current study suggests that heat drying improves the production of ganoderic acids by the upregulation of TCA-related pathways, which, in turn, gives a significant reduction in the inflammatory response of LPS-induced BV2 cells. This may be attributed to the inhibition of NF-κB and MAP kinase signaling pathways in cells treated with heat-dried extracts.


2002 ◽  
Vol 184 (4) ◽  
pp. 1172-1179 ◽  
Author(s):  
Thomas M. A. Gronewold ◽  
Dale Kaiser

ABSTRACT Cell-bound C-signal guides the building of a fruiting body and triggers the differentiation of myxospores. Earlier work has shown that transcription of the csgA gene, which encodes the C-signal, is directed by four genes of the act operon. To see how expression of the genes encoding components of the aggregation and sporulation processes depends on C-signaling, mutants with loss-of-function mutations in each of the act genes were investigated. These mutations were found to have no effect on genes that are normally expressed up to 3 h into development and are C-signal independent. Neither the time of first expression nor the rate of expression increase was changed in actA, actB, actC, or actD mutant strains. Also, there was no effect on A-signal production, which normally starts before 3 h. By contrast, the null act mutants have striking defects in C-signal production. These mutations changed the expression of four gene reporters that are related to aggregation and sporulation and are expressed at 6 h or later in development. The actA and actB null mutations substantially decreased the expression of all these reporters. The other act null mutations caused either premature expression to wild-type levels (actC) or delayed expression (actD), which ultimately rose to wild-type levels. The pattern of effects on these reporters shows how the C-signal differentially regulates the steps that together build a fruiting body and differentiate spores within it.


1948 ◽  
Vol 21 (4) ◽  
pp. 853-859
Author(s):  
R. F. A. Altman

Abstract As numerous investigators have shown, some of the nonrubber components of Hevea latex have a decided accelerating action on the process of vulcanization. A survey of the literature on this subject points to the validity of certain general facts. 1. Among the nonrubber components of latex which have been investigated, certain nitrogenous bases appear to be most important for accelerating the rate of vulcanization. 2. These nitrogen bases apparently occur partly naturally in fresh latex, and partly as the result of putrefaction, heating, and other decomposition processes. 3. The nitrogen bases naturally present in fresh latex at later stages have been identified by Altman to be trigonelline, stachhydrine, betonicine, choline, methylamine, trimethylamine, and ammonia. These bases are markedly active in vulcanization, as will be seen in the section on experimental results. 4. The nitrogenous substances formed by the decomposition processes have only partly been identified, on the one hand as tetra- and pentamethylene diamine and some amino acids, on the other hand as alkaloids, proline, diamino acids, etc. 5. It has been generally accepted that these nitrogenous substances are derived from the proteins of the latex. 6. Decomposition appears to be connected with the formation of a considerable amount of acids. 7. The production of volatile nitrogen bases as a rule accompanies the decomposition processes. These volatile products have not been identified. 8. The active nitrogen bases, either already formed or derived from complex nitrogenous substances, seem to be soluble in water but only slightly soluble in acetone.


1967 ◽  
Vol 45 (11) ◽  
pp. 2137-2153 ◽  
Author(s):  
A. Fuchs ◽  
R. Rohringer ◽  
D. J. Samborski

Wheat leaves infected with stem rust, especially those of susceptible plants, contained more phenylalanine and tyrosine than healthy leaves. The utilization of phenylalanine was increased in both the susceptible and resistant reaction, but the utilization of tyrosine was increased only in the susceptible reaction. No evidence of interconversion of these amino acids was obtained.In n-butanol extracts, which contained glycosides, many constituents were labelled after feeding of L-phenylalanine-U-14C. Most of the n-butanol extractives from resistant-reacting leaves contained more label than those from susceptible-reacting leaves or from healthy leaves. However, one of the n-butanol extractives from susceptible-reacting leaves was 5–10 times as active as that isolated from the other tissues.With L-phenylalanine-U-14C and ferulate-U-14C as precursors, more activity was recovered in insoluble than in soluble esters (of ferulate and p-coumarate). With L-tyrosine-U-14C as precursor, the reverse was observed. After infection, the proportion of label in insoluble esters increased more in resistant leaves than it did in susceptible leaves, regardless of the precursor used.A major portion of the activity from these precursors was recovered in the insoluble residue that contained protein and other polymers. In the experiment with L-phenylalanine-U-14C, this residue was fractionated into protein and non-hydrolyzable material. Susceptible-reacting leaves contained equal amounts of activity in these fractions, while resistant-reacting leaves incorporated 2.5 times as much activity into the non-hydrolyzable material as into protein.


1976 ◽  
Vol 154 (1) ◽  
pp. 43-48 ◽  
Author(s):  
J D Young ◽  
J C Ellory ◽  
E M Tucker

1. Uptake rates for 23 amino acids were measured for both normal (high-GSH) and GSH-deficient (low-GSH) erythrocytes from Finnish Landrace sheep. 2. Compared with high-GSH cells, low-GSH cells had a markedly diminished permeability to D-alanine, L-alanine, α-amino-n-butyrate, valine, cysteine, serine, threonine, asparagine, lysine and ornithine. Smaller differences were observed for glycine and proline, whereas uptake of the other amino acids was not significantly different in the two cell types.


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