• 임산에너지
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• 제23권2호
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• pp.21-28
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• 2004

표고버섯 톱밥재배시 배양에 의한 중량감소율과 생장기간에 따른 에르고스테롤 정량으로 균사 생장량을 조사하였고, 배양기간과 자실체 발생기간에 따른 균체 외와 균체 내의 효소 특성을 조사하였다. 배양기간에 따른 중량 감소는 산림5호가 농기3호와 산림6호에 비해 낮은 중량감소율을 나타냈다. 에르고스테롤 정량에 의한 균사 생장량 조사 결과, 암배양기간 동안 3균주 모두 균사 생장량이 증가하였으며, 농기3호가 상대적으로 높은 증가율을 보인 반면, 산림5호는 낮은 증가율을 보였다. 농기3호와 산림6호는 명배양기간 동안에 균사 생장량이 최고치에 이르렀으며, 산림5호는 자실체 발생기간 전까지 계속 증가하였다. 배양기간과 발생기간에 따른 글체 외와 군체 내 효소 역가를 측정한 결과, 배양 초기(10일)에는 셀룰로오스와 헤미셀룰로오스 분해에 관여하는 CMCase, avicelase, xylanase, glucanase의 역가가 높았고, 배양 10일 후 리그닌 분해에 관여하는 laccase와 Mn-peroxidase의 역가가 높아지는 경향을 나타내었다.

• Journal of the Korean Wood Science and Technology
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• 제32권1호
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• pp.28-34
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• 2004

본 연구는 자기가수분해전 처리를 통하여 제조한 반응성이 높은 셀룰로오스(high reactive cellulose, HRC)기질의 카르복시메틸화(carboxymethylation, CM화) 특성을 알기 위하여 수행되었으며, 비교를 위하여 시판 알파셀룰로오스(commercial α-cellulose, CAC) 및 침엽수 리파이나기계펄프(Refiner mechanical pulp, RMP) 2종의 시료를 사용하였다. HRC는 12시간 당화처리로 70%, 24시간 처리로 90%, 72시간 처리로 99.5%의 높은 당화율을 나타냈다. 아울러 Cellulase 효소활성에 있어서 처리 전후에 측정된 CMCase 및 Avicelase의 효소활성의 큰 변화가 없었다. 이에 대하여 72시간 처리로 CAC는 57%의 당화율을, 리그닌을 많이 포함하는 RMP는 38%의 매우 낮은 당화율을 보였다. CM화시 리그닌함량이 낮은 HRC 및 CAC시료의 CM화가 용이하였고, 1.13-1.15의 높은 치환도를, 리그닌함량이 많은 RMP는 0.85 정도의 낮은 치환도를 나타냈다. 모든 시료에서 알칼리의 농도는 30%, 3시간 처리가 가장 높은 치환도를 보여주었다. CM화물로부터의 수용성부분은 HRC 및 CAC에서 98-98.5%, RMP 로부터는 31.5%로 매우 낮았다. 비표면적이 낮은 RMP는 보수도가 매우 낮았으며, 비표면적이 높았던 CAC 및 HRC는 435% 및 321%의 매우 높은 보수도 값을 나타냈다. 팽윤도에 있어서는 비표면적과는 무관하게 HRC, RMP 그리고 CAC 순으로 팽윤율이 커졌다.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2001년도 추계학술발표대회
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• pp.629-632
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• 2001

자연계로부터 분리된 FJ1의 환경변수 및 기질 특이성을 본 연구에서 살펴보았는데, 분리 균주 FJ1의 특성은 최적pH, 최적온도는 각각 $6{\sim}7$, $25{\sim}30^{\circ}C$이었다. 또한, 분리균주는 FJ는 Avicel, 섬유소페기물과 같은 결정성 섬유소물질의 분해에 유리함을 알 수 있었다. 본 연구에서는 cellulose의 분해에 관련된 효소를 분비하는 분리균주 FJ1의 환경변수 및 기질 특이성을 조사하였고, 이를 기본으로 하여 배양인자의 조절을 통한 최적의 효소생산 및 생산되어진 효소에 의한 섬유소 페기물(볏짚, 폐지, 음식물 쓰레기 등)의 당화 특성을 검토하고 있다.

• Journal of Microbiology and Biotechnology
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• 제13권1호
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• pp.1-8
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• 2003

Strain FJI, a filamentous fungus isolated from rotten wood, showed high ability to hydrolyze cellulosic materials. To identify the strain FJI, ITS sequencing analysis and morphological observation were performed. The strain FJI was identified as Trichoderma harzianum. The strain produced a large amount of CMCase, xylanase, ${\beta}-glucosidase$, and avicelase. Optimal culture conditions for the production of the enzymes, such as pH, temperature, and inoculation concentration, were initial pH 6.0-7.0,$25-30^{\circ}C$, and $10^4$ ea-spores/ml in Mandel's medium, respectively. T.hanzianum FJI utilized various cellulosic materials and organic nitrogen sources to produce cellulases and xylanase, and also considerably a crystalline and/or insoluble material like Avicel and rice straw. The highest levels of CMCase and xylanase were 41.2 and 65.6 U/ml in 7 days of cultivation using 2.5% of carbon source (Avicel+CMC) and 0.5% of nitrogen source (peptone), respectively.

• 한국미생물·생명공학회지
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• 제25권4호
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• pp.346-353
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• 1997

During the screening of cellulase producing microorganisms, a fungal strain C-4 was selected from etiolated leaves. Based on taxonomic studies, the fungus could be classified as a strain of Trichoderma sp. When the strain C-4 was cultured in Mandels' media at 28$circ$C for 6 days, the enzyme activities detected in broth were as follows: 8.2 U/ml (28.1 U/mg) of CMCase activity, 0.75 U/ml (2.58 U/mg) of Avicelase activity, 1.67 U/ ml (5.68 U/mg) of $eta$-glucosidase activity. The optimum pH for enzyme induction was 6.2. The crude enzyme retained 100% of its original CMCase activity at 50$circ$C for 1 hr (pH 5.0), and at 4$circ$C for 24 hrs (pH 5.0). There was no effect on the CMCase activity in the presence of 1 mM of CsCl, LiCl, MgCl$_{2}$, and FeCl$_{2}$, respectively. When the crude enzyme was treated with trypsin and chymotrypsin (2% W/w) for 10 minutes, the remaining CMCase activity was 70%, but there was no further loss of activity for 60 minutes treatment at 30$circ$C. The crude enzyme showed the synergism with rumen fluid for the hydrolysis of Avicel and CMC by 118% and 130%, respectively.

• Journal of Microbiology and Biotechnology
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• 제22권11호
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• pp.1501-1509
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• 2012

A novel bacterial strain, MG7, with high cellulase activity was isolated and identified by morphological characteristics and molecular phylogeny analysis as Paenibacillus barcinonensis. Maximum production of cellulase by MG7 was observed at pH 7.0 and $35^{\circ}C$. The enzyme was purified with a specific activity of 16.88 U/mg, the cellulase activity was observed in a zymogram, and its molecular mass (58.6 kDa) was confirmed by SDS-PAGE. The purified enzyme showed maximum activity at pH 6.0 and $65^{\circ}C$ and degraded cellulosic substrates such as carboxy methyl cellulose (CMC), Avicel, filter paper, and ${\beta}$-glucan. The enzyme showed stability with 0.5% concentration of various surfactants. The $K_m$ and $V_{max}$ of cellulase for CMC and Avicel were found to be 0.459mg/ml and 10.46mg/ml/h, and 1.01 mg/ml and 10.0 mg/ml/h, respectively. The high catalytic activity and its stability to temperature, pH, surfactants, and metal ions indicated that the cellulase enzyme by MG7 is a good candidate for biotechnological applications.

• 한국미생물·생명공학회지
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• 제18권4호
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• pp.383-389
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• 1990

Penicillium verruculosum 섬유소 분해효소의 유도물질인 KC-flock 및 cellobiose octaacetate(COA)를 유일한 탄소원으로 포함하는 배지에서 21일간 배양하면서 배양여액 중의 섬유소 분해효소 각 성분의 활성도와 전기영동상의 단백질 양상을 검토하였다. 배양여액의 중의 총단백질 생성 및 섬유소 분해활성의 유도 효과는 COA 배지가 다른 두 배지의 3배 이상이었다. 배양기간의 증가에 따라 배양여액 중의 총단백질량이 증가되었는데 CMC 분해활성이나 $\beta$-glucosidase 활성의 증가보다는 avicel 분해활성도의 증가가 총단백질량의 증가와 유사하다.

• Mycobiology
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• 제36권1호
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• pp.74-76
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• 2008

To obtain basic information on the biochemical property of basidiospores of shiitake mushroom (Lentinula edodes), the ability of producing extracellular enzyme was assessed using a chromogenic plate-based assay. For the aim, amylase, avicelase, $\beta$-glucosidase, CM-cellulase, pectinase, proteinase, and xylanase were tested against monokaryotic strains generated from forty basidiospores of two different parental dikaryotic strains of shiitake mushroom, Sanjo-101Ho and Sanjo-108Ho. These two parental strains showed different degree of extracellular enzyme activity. No identical patterns of the degree of enzyme activity were observed between monokaryotic strains and parental strains of the two shiitake cultivars. The degree of extracellular enzyme activity also varied among monokaryotic strains of the two shiitake cultivars. Our results showed that dikaryotic parental strains of shiitake mushroom produce monokaryotic basidiospores having very diverse biochemical properties.

• Journal of Microbiology and Biotechnology
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• 제26권5호
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• pp.909-917
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• 2016

The shiitake mushroom industry has suffered from Camptomyia (gall midges) pest, which feeds on the mycelium of shiitake mushroom during its cultivation. It has been postulated that fungal damage of shiitake bed-logs is associated with infestation by the insect pest, but this is not well understood. To understand the fungal damage associated with Camptomyia pest, various Trichoderma species were isolated, identified, and characterized. In addition to two previously known Trichoderma species, T. citrinoviride and T. deliquescens, two other Trichoderma species, T. harzianum and T. atroviride, were newly identified from the pestinfested bed-log samples obtained at three mushroom farms in Cheonan, Korea. Among these four species, T. harzianum was the most evident. The results of a chromogenic media-based assay for extracellular enzymes showed that these four species have the ability to produce amylase, carboxyl-methyl cellulase, avicelase, pectinase, and ß-glucosidase, thus indicating that they can degrade wood components. A dual culture assay on PDA indicated that T. harzianum, T. atroviride, and T. citrinoviride were antagonistic against the mycelial growth of a shiitake strain (Lentinula edodes). Inoculation tests on shiitake bed-logs revealed that all four species were able to damage the wood of bed-logs. Our results provide evidence that the four green mold species are the causal agents involved in fungal damage of shiitake bed-logs infested by Camptomyia pest.

• Mycobiology
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• 제43권1호
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• pp.81-86
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• 2015

To promote the selection of promising monokaryotic strains of button mushroom (Agaricus bisporus) during breeding, 61 progeny strains derived from basidiospores of two different lines of dikaryotic parental strains, ASI1038 and ASI1346, were analyzed by nucleotide sequencing of the intergenic spacer I (IGS I) region in their rDNA and by extracellular enzyme assays. Nineteen different sizes of IGS I, which ranged from 1,301 to 1,348 bp, were present among twenty ASI1346-derived progeny strains, while 15 different sizes of IGS I, which ranged from 700 to 1,347 bp, were present among twenty ASI1038-derived progeny strains. Phylogenetic analysis of the IGS sequences revealed that different clades were present in both the ASI10388- and ASI1346-derived progeny strains. Plating assays of seven kinds of extracellular enzymes (${\beta}$-glucosidase, avicelase, CM-cellulase, amylase, pectinase, xylanase, and protease) also revealed apparent variation in the ability to produce extracellular enzymes among the 40 tested progeny strains from both parental A. bisporus strains. Overall, this study demonstrates that characterization of IGS I regions and extracellular enzymes is useful for the assessment of the substrate-degrading ability and heterogenicity of A. bisporus monokaryotic strains.