Fruiting body of Paecilomyces fumosoroseus formed on unpolished rice medium supplemented with 20% (w/w) silkworm pupae after 40 days of incubation at 25 o C under 100 lux. 

Fruiting body of Paecilomyces fumosoroseus formed on unpolished rice medium supplemented with 20% (w/w) silkworm pupae after 40 days of incubation at 25 o C under 100 lux. 

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The fruiting body of Paecilomyces fumosoroseus was collected at Mt. Mani, Ganghwa Island, Korea in September, 2001. This study was carried out to obtain the basic informations for the mycelial growth and fruiting body production of P. fumosoroseus in artificial media. The optimal conditions for the mycelial growth were obtained at 25℃ and in the ra...

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... conditions of P. fumosoroseus. Effect of pH: The pH value suitable for a favorable growth of P. fumosoroseus was obtained in the range of pH 6~9. Choi et al. (1999) reported that mycelial growth of P. japonica was optimal at pH 7. Shim et al. (2003) also reported that P. sinclairii showed maximal mycelial growth at pH 8. However, the mycelial growth and den- sity of P. fumosoroseus was almost identical in the range of pH 6~9 (Fig. 2). These results suggest that P. fumoso- roseus may have a broad pH range for its favorable myce- lial growth in nature. Effect of temperature: The temperature suitable for the mycelial growth of P. fumosoroseus was obtained at 25 o C (Fig. 3) and the result was similar to that of Lee et al. (1999). Lee et al. (1999) reported that the mycelial growth of P. fumosoroseus had been expedited gradually in pro- portion to the rise of temperature and was the most suit- able at 25 o C. Even though the mycelial growth of P. fumosoroseus was favorable at the range of 20 to 25 o C and had been expedited in proportion to the rise of tem- perature, the mycelial growth appeared to be suppressed at the temperature higher than 30 o C (Fig. 3). Since most of entomopathogenic fungi has been known to complete their life cycle under the humid, cool deposits covered with fallen leaves ( Sung et al., 1997), it is reasonable to pre- dict that the mycelial growth of P. fumosoroseus was good in the temperature range of 20~25 o C. Screening of favorable culture media: Ten different culture media were used to screen the optimal mycelial growth of P. fumosoroseus. Of 10 culture media, Hamada medium was the most suitable for a favorable growth of P. fumosoroseus (Table 2). This result is corresponded with that of P. sinclairii which had been reported by Shim et al. (2003). Even though the mycelial growth of P. fumosoroseus and P. sinclairii was optimal on Hamada medium, the mycelial growth of Grifola umbellata was very poor on Hamada medium. This contradictory result indicates that taxonomically distinct fungal groups may have different nutritional requirement. Even though the mycelial growth in 10 different media showed wide range of variations (55.5~77.0 mm), the mycelial density were compact in 9 of 10 culture media tested ( Table 2). Effect of carbon and nitrogen sources: Dextrin and histidine were screened as suitable carbon and nitrogen source for the mycelial growth of P. fumosoroseus (Table 3 and Table 4). The colony diameter of P. fumosoroseus after 14 days of incubation were recorded 78.0 mm in dextrin and 74.5 mm in histidine containing basal media, respectively. The mycelial density of P. fumosoroseus showed thin appearances in all carbon source, whereas compact appearances were observed in 16 nitrogen sources. Shim et al. (2003) also reported that P. sinclairii grew very well in basal medium which contained dextrin and glutamine, respectively. Since P. fumosoroseus and P. sinclairii belong to genus Paecilomyces of Hypho- mycetes, Deuteromycota, they are taxonomically consid- ered as very close species (Lacey et al., 1999). However, the nutritional requirement for the mycelial growth of P. fumosoroseus and P. sinclairii seems to be different. Effect of C/N ratio: Optimum C/N ratio suitable for a favorable growth of P. fumosoroseus was observed on the culture media which were adjusted to C/N ratio of 40:1. On the culture media which were mixed with 1% glucose as carbon source and then adjusted to the ratio of 30:1, P. sinclairii showed the most favorable mycelial growth (Shim et al., 2003). Despite a gradual rise of 1%, 2%, 3% and 4% glucose, C/N ratio of 40:1 showed the most favorable mycelial growth of P. fumosoroseus as com- pared with other C/N ratios ( Table 5). Effect of cereal extract media: Sung et al. (1993) reported that the mycelial growth of Cordyceps militaris was favorable on the artificial medium supplemented with silkworm pupae, rice powder or wheat powder. Shim et al. (2003) also reported that silkworm pupae supple- mented to the cereal extract medium showed favorable mycelial growth of P. sinclairii. The mycelial growth of P. fumosoroseus was optimal on corn meal agar supple- mented with 10~30% of silkworm pupae (Table 6). Partic- ularly, the mycelial growth of P. fumosoroseus recorded 71.9 mm in PDA plate with maximal value on corn meal agar supplemented with 30% of silkworm pupae. Based on these results, silkworm pupae may contain good nutritional sources to promote mycelial growth of P. fumosoroseus. Formation of fruiting body: The fruiting body of P. fumosoroseus was formed abundantly on an unpolished rice medium supplemented with 20% (w/w) silkworm pupae at 25 o C under 100 lux (Fig. 1, Table 7). Shim et al. (2003) reported that fruiting body of P. sinclairii was formed after 10 days of incubation at 25 o C under 500 lux. The fruiting body of P. fumosoroseus was formed after 12 days of incubation at 25 o C under light condition. But, unlike the P. sinclairii, the fruiting body of P. fumosoro- seus was formed more abundantly under 100 lux than 500 lux. The fruiting body of P. fumosoroseus was not formed at 30 o C. This result also coincide with mycelial growth of the fungi which was suppressed at 30 o C (Fig. 3). Even though P. fumosoroseus have been considered as a good candidate for biocontrol of insect pests, there has been no report that P. fumosoroseus was used commer- cially for the biocontrol agent in Korea (Altre et al., 1999;Cantone and Vandenberg, 1999;Lacey et al., 1999;Lee et al., 1999;Nam et al., 2000). To develop P. fumosoro- seus as a mycoinsecticide, it is necessary to develop culture method to produce fruiting bodies in in vitro condition. In this study, the conditions for optimal myce- lial growth and fruiting body formation of P. fumosoro- seus was developed for the first time in Korea. Thus, the basic information obtained from this study can be used for the mass production of fruiting bodies of P. fumosoroseus. ...

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... The optimal C/N ratio suitable for the mycelial growth may vary according to species. For instance, the suitable ratios for the enhanced mycelial growth of Cystoderma amianthinum [21], Macrolepiota procera [22], Oudemansiella radicata [23], Paecilomyces fumosoroseus [24], and Ganoderma applanatum [25] were found to be 30:1, 10:1, 20:1, 40:1, and 2:10, respectively. Our result indicated that a C/N ratio of 3:1 was optimal for mycelial growth of T. versicolor, which is in high agreement with studied by Jo et al. [1]. ...
... This result suggested that C. molybdites can be incubated at a temperature between 24 and 28°C to attain the optimum mycelial biomass production. Similarly, Shim et al. [39] reported that the mycelial growth of Paecilomyces fumosoroseus had been expedited gradually in proportion to the rise of temperature and the growth was most suitable at 25°C. Kim et al. [40] revealed that the temperature suitable for the mycelial growth of Oudemansiella radicata was at 25°C. ...
... Radial growth of P.erengii and P. florida recorded 5 cm in CDA medium. In general, CDA medium gave lower values of radial growth for tested mushroom strains after 6 days of incubation (Shim et al 2003). Such differences in mycelial growth detected on the tested agar media may be due to the availability of different carbon sources and other required nutrients. ...
... The best mycelial growth of both white and brown strains of H. marmoreus was found at 20°C. The both strains of H. marmoreus love medium-low temperature for adequate vegetative proliferation. Lee et al. (1999) and Shim et al. (2003) reported that the mycelial growth of Paecilomyces fumosoroseus had been expedited gradually in proportion to the rise of temperature and the most suitable was at 25°C. Even though the mycelial growth of P. fumosoroseus was favorable at the range of 20-25°C and had been expedited in proportion to the rise of temperature, the mycelial growth appeared to be suppressed at the temperature higher than 30°C. ...
... Choi et al. (1999) and Chi et al. (1996) reported that mycelial growth of Phellinus japonica and P. linteus was optimal at pH 7 and 6-7, respectively. Shim et al. (2003) exposed that optimal pH was 8 for Paecilomyces sinclairii. Imtiaj et al. (2008a) observed the pH requirement for the vegetative growth of 10 strains of Schizophyllum commune and reported that pH 5 was the best. ...
... This result suggested that mushrooms may have a broad pH range for their optimal mycelial growth in nature. The results of this study is completely similar to Shim et al. (2005), Shim et al. (2003), Choi et al. (1999) and Chi et al. (1996). ...
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Hypsizygus marmoreus is an edible and medicinal mushroom belongs to Basidiomycetes. The optimal culture conditions for the vegetative growth of brown and white strains of H. marmoreus were investigated to obtain suitable farming condition. Temperature suitable and unsuitable for vegetative growth was obtained at 20 and 35°C, respectively. The both strains of H. mermoreus love medium temperature and the mycelial growth was well developed at 20-25°C. This mushroom prefer pH ranging 6-8 for mycelial growth. The highest and lowest mycelial growth was found at pH 7 and 5 of both strains, respectively. Among 5 different carbon sources, sucrose was the best, whereas, maltose and lactose were the worst. The most suitable nitrogen sources were CaNO, (in brown strain 65.6 mm and in white strain 56.3 mm) and the most unsuitable was NH4HPO4 (in brown strain 44.02 mm and in white strain 40.2 mm). Five different culture media were used to screen the optimal mycelial growth of H. marmoreus. PDA and YM (yeast-malt extract) were the most suitable and Czapek dox and Hennerberg were the most unfavorable for vegetative growth, whereas, glucose peptone was moderately suitable. The highest and lowest vegetative growth was observed in media prepared with mango (Mangifera indica) and koroi (Albizia procera) sawdust, respectively. However, for both strains, 3 weeks were required to complete mycelium running in mango sawdust, whereas, 4 weeks were spent to get 100% mycelium running in mahagoni (Swietenia mahagoni) and koroi sawdust. The premordia and fruiting bodies of H. marmoreus were formed in the mango sawdust medium sooner. The fruiting bodies of brown strain were formed earlier than white strain after occurrence of primordia. In case of limiting ventilation, the stem development was found to be good but no cap was seen to be formed. Ventilation influenced the growth and development of fruit body of H. marmoreus. Therefore, it could be said that physiochemical requirement for the vegetative growth is strictly considerable and results focused in this paper could be followed by farmers to scale up farming of H. marmoreus in Bangladesh.
... In this study, conidia production was reduced when 26 % oxygen pulses were applied, regardless of the culture system. This might be explained by different media, inoculum size and culture system, which have important effects on growth physiology and conidia production (Pham et al. 2010; Rodríguez-Gómez et al. 2009; Shim et al. 2003). The time when light (Sánchez-Murillo et al. 2004) or oxidant pulses (Garcia-Ortiz et al. 2015) are applied determines whether stimuli affect conidiation. ...
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Conidia production and quality from mycoinsecticides in solid-state cultures (SSC) are frequently inferred from superficial culture (SC) results. Both parameters were evaluated for two Isaria fumosorosea strains (ARSEF 3302 and CNRCB1), in SC and SSC, using culture media with the same chemical composition. For both strains, conidia production was higher in SC than SSC in terms of conidia per gram of dry substrate. Germination in both strains did not show significant differences between SC and SSC (>90 %). Similarly, conidia viability in ARSEF 3302 strain did not show differences at early stages between SC and SSC, but was higher in SC compared to SSC in the late stage of culture; in contrast, conidia from CNRCB1 strain did not differ between both culture systems. Some infectivity parameters improved in conidia from SSC, compared to SC at the early stages, but these differences disappeared at the final stage, independently of the strain. Both strains showed decreased conidia production when 26 % O2 pulses were applied; nevertheless, conidiation in SSC was two orders of magnitude more sensitive to oxidant pulses. In SC with 26 % O2 pulses, conidia viability for both strains at early stages, was higher than in normal atmospheric conditions. Infectivity towards Galleria mellonella larvae was similar between conidia from normal atmosphere and oxidant conditions; notably, for the strain ARSEF 3302 infectivity decreased at the final stage. This study shows the intrinsic differences between SC and SSC, which should be considered when using SC as a model to design production processes in SSC.
... Two different liquid culture using P. fumosoroseus were tested for biocontrol efficacy using basal salts medium (Sandoval-Coronado et al., 2001). Another ten different culture media were used to investigate a mycelia growth of P. fumosoroseus, where, only two media were the favorable carbon and nitrogen source for maximal growth (Shim et al., 2003). Recently, the growth of P. hepiali in various agar media was studied, where, the addition of peptone improved mycelial growth and the most favorable carbon sources were mannose, fructose and glucose (Chioza, and Ohga, 2013). ...
Article
Objective: Marine fungi play an important role in human and animal health, leading compounds to new drug discoveries and prospects for their bioactivity potential. Materials and Methods: Paecilomyces WE3-F was isolated from marine sediment (Red Sea, Shalateen, Egypt). Fungal isolate was screened for their antagonistic activity against four Gram-positive (Bacillus cereus, Lesteria monocytogenes, Micrococcus luteus and Staphylococcu aureus) and four Gram-negative (Aeromonas hydrophila, Flavobacteruim sp, Pseudomonas aeruginosa and Vibrio cholera,) pathogenic bacteria. Paecilomyces WE3-F was identified using 18S rRNA technology. Seven factors were chosen to be screened for bioactivity using the Placket Burman experimental design: sucrose, yeast extract, Na NO3, temperature, initial pH, inoculum size, and incubation period. Results: Among conditional factors, acidic pH and 1.5 ml inoculum size favored the bioactive metabolites. Furthermore, a number of solvents have been experimented for the extraction of the bioactive metabolite(s). Dichloromethane (DCM) crude extract from the fermentation broth of a marine Paecilomyces WE3-F showed the highest activity with averages of 26 and 24 mm against G-ve and G+ve, respectively. Under optimal culture conditions, the maximum extractable compound concentration in a 10-L culture medium reached 83.4 mg/L. Based on data obtained by thin layer chromatogram (TLC), gas chromatography - mass spectrum (GC-MS) and Fourier Transform Infrared (FTIR) the major compound, betulin was structurally identified. Conclusions: The isolated marine Paecilomyces WE3-F, therefore, showed the ability to produce a betulin yield after optimal operating conditions for antibacterial potential.
... Two different liquid culture using P. fumosoroseus were tested for biocontrol efficacy using basal salts medium (Sandoval-Coronado et al., 2001). Another ten different culture media were used to investigate a mycelia growth of P. fumosoroseus, where, only two media were the favorable carbon and nitrogen source for maximal growth (Shim et al., 2003). Recently, the growth of P. hepiali in various agar media was studied, where, the addition of peptone improved mycelial growth and the most favorable carbon sources were mannose, fructose and glucose (Chioza, and Ohga, 2013). ...
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Objective: Marine fungi play an important role in human and animal health, leading compounds to new drug discoveries and prospects for their bioactivity potential. Materials and Methods: Paecilomyces WE3-F was isolated from marine sediment (Red Sea, Shalateen, Egypt). Fungal isolate was screened for their antagonistic activity against four Gram-positive (Bacillus cereus, Lesteria monocytogenes, Micrococcus luteus and Staphylococcu aureus) and four Gram-negative (Aeromonas hydrophila, Flavobacteruim sp, Pseudomonas aeruginosa and Vibrio cholera,) pathogenic bacteria. Paecilomyces WE3-F was identified using 18S rRNA technology. Seven factors were chosen to be screened for bioactivity using the Placket Burman experimental design: sucrose, yeast extract, Na NO3, temperature, initial pH, inoculum size, and incubation period. Results: Among conditional factors, acidic pH and 1.5 ml inoculum size favored the bioactive metabolites. Furthermore, a number of solvents have been experimented for the extraction of the bioactive metabolite(s). Dichloromethane (DCM) crude extract from the fermentation broth of a marine Paecilomyces WE3-F showed the highest activity with averages of 26 and 24 mm against G-ve and G+ve, respectively. Under optimal culture conditions, the maximum extractable compound concentration in a 10-L culture medium reached 83.4 mg/L. Based on data obtained by thin layer chromatogram (TLC), gas chromatography-mass spectrum (GC-MS) and Fourier Transform Infrared (FTIR) the major compound, betulin was structurally identified. Conclusions: The isolated marine Paecilomyces WE3-F, therefore, showed the ability to produce a betulin yield after optimal operating conditions for antibacterial potential.
... Two different liquid culture using P. fumosoroseus were tested for biocontrol efficacy using basal salts medium (Sandoval-Coronado et al., 2001). Another ten different culture media were used to investigate a mycelia growth of P. fumosoroseus, where, only two media were the favorable carbon and nitrogen source for maximal growth (Shim et al., 2003). Recently, the growth of P. hepiali in various agar media was studied, where, the addition of peptone improved mycelial growth and the most favorable carbon sources were mannose, fructose and glucose (Chioza, and Ohga, 2013). ...
Article
Full-text available
Objective: Marine fungi play an important role in human and animal health, leading compounds to new drug discoveries and prospects for their bioactivity potential. Materials and Methods: Paecilomyces WE3-F was isolated from marine sediment (Red Sea, Shalateen, Egypt). Fungal isolate was screened for their antagonistic activity against four Gram-positive (Bacillus cereus, Lesteria monocytogenes, Micrococcus luteus and Staphylococcu aureus) and four Gram-negative (Aeromonas hydrophila, Flavobacteruim sp, Pseudomonas aeruginosa and Vibrio cholera,) pathogenic bacteria. Paecilomyces WE3-F was identified using 18S rRNA technology. Seven factors were chosen to be screened for bioactivity using the Placket Burman experimental design: sucrose, yeast extract, Na NO3, temperature, initial pH, inoculum size, and incubation period. Results: Among conditional factors, acidic pH and 1.5 ml inoculum size favored the bioactive metabolites. Furthermore, a number of solvents have been experimented for the extraction of the bioactive metabolite(s). Dichloromethane (DCM) crude extract from the fermentation broth of a marine Paecilomyces WE3-F showed the highest activity with averages of 26 and 24 mm against G-ve and G+ve, respectively. Under optimal culture conditions, the maximum extractable compound concentration in a 10-L culture medium reached 83.4 mg/L. Based on data obtained by thin layer chromatogram (TLC), gas chromatography-mass spectrum (GC-MS) and Fourier Transform Infrared (FTIR) the major compound, betulin was structurally identified. Conclusions: The isolated marine Paecilomyces WE3-F, therefore, showed the ability to produce a betulin yield after optimal operating conditions for antibacterial potential.
... The following 10 nitrogen sources were tested: alanine, urea, glycine, calcium nitrate, potassium nitrate, methionine, histidine, arginine, ammonium phosphate and ammonium acetate. Each nitrogen source was added with 20 g of glucose to the basal medium at the concentration of 0.02 M as described by Shim et al. [14]. The basal medium was adjusted to pH 6 before autoclaving at 121˚C for 15 minutes. ...
... The most suitable temperature for mycelial growth of S. crispa was found to be 25˚C (Figure 2). This temperature is reported as the most favourable for the majority of mushrooms which include Coprinus comatus [15], Paecilomyces hepiali [12], Paecilomyces fumosoroseus [14] [16], Ophiocordyceps heteropoda [17] and Cordyceps cardinalis [18]. The next favourable temperature was 20˚C. ...
... Modified mushroom complete medium (MMCM) was used for this experiment. The mushroom complete medium (20.0 g glucose, 2.0 g peptone, 2.0 g yeast extract, 1 g K 2 HPO 4 , 0.5 g MgSO 4 , 0.5 g KH 2 PO 4 , 20.0 g agar and 1000 ml distilled water) in Shim et al. [14] was modified by removing 2 grams of yeast extract and raising the quantity of peptone from 2 to 4 grams to make MMCM. A medium for each carbon source was prepared by adding 20 g to the MMCM to replace glucose. ...
Article
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Growth of ”Paecilomyces hepiali” in various agar media and yield of fruit bodies in rice based media were studied. The best growth in agar media was obtained at 25°C (61.86 mm colony diameter in 14 days). The initial agar media pH range from 6 to 8 was found to be the most favourable for mycelial growth. This study found that agars made with powders of cereal grains alone do not support good mycelial growth of ”P. hepialid”. Addition of peptone improved mycelial growth significantly. The most favourable carbon sources were Mannose, Fructose and Glucose. Organic nitrogen sources were found to be the most preferred. The results demonstrated that brown rice is better than polished rice in yield of fruit bodies. Addition of peptone was found to be quite significant in enhancing yield of fruit bodies. Peptone, as a supplement, gave a better yield than addition of egg yolk, albumen and a mixture of the two. The medium with 40 g brown rice, 0.325 g glucose, 0.65 g sucrose, 2 g peptone and 65 ml corn steep liquor was found to be the most favourable and it yielded 19.3 g of fresh fruit bodies.