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一株纤维素降解真菌的筛选及鉴定 被引量:32

Isolation and identification of a cellulose degrading fungi
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摘要 【目的】分离筛选高效降解纤维素的真菌菌株,并研究其产酶能力。【方法】利用刚果红染色法从甘蔗地土壤中分离纤维素降解真菌,再通过测定滤纸的降解率及发酵酶活复筛。【结果】综合考虑水解圈,水解圈和菌株直径的比值(HC值),滤纸的降解率和复筛酶活,对试验真菌降解纤维素的能力进行综合评价,筛选到具有较强纤维素降解能力的真菌菌株SJ1,经形态学观察及分子生物学鉴定,该菌属于草酸青霉。其滤纸酶活、内切葡聚糖酶酶活(CMC酶活)、β-葡聚糖苷酶酶活和外切葡聚糖酶酶活(CBH酶活)分别为25.15、740.42、58.03和2.442 U/mL。【结论】菌株SJ1是一株十分具有研究开发潜力的纤维素酶生产菌株。 Objective The aim of this study was to screen efficient cellulose degrading strains and to investigate their cellulase-producing conditions. Methods The fungus were screened from sugarcane soil by using the Congo red dye test, then measured the degradation rate of filter paper and the enzyme activity for second-screening. [Results] The hydrolyzation zone, clearing zone ratios (clearing zone diameter/colony diameter), the degradation rate of filter paper and cellulose activity were taken as evaluating selection criteria. We isolated one fungi with cellulose degrading ability, of which S J1 was identified as Penicillium oxalicum by morphological and molecular technology. The results showed that the filter paper activity (FPA), endoglucanase activity (CMCase activity), β-glucosidase activity and exoglucanase activity (CBH activity) of SJ1 were 25.15 U/mL, 740.42 U/mL, 58.03 U/mL and 2.442 U/mL, respectively. [Conclusion] Strain S J1 was a cellulase-producing strain with broad development potential.
出处 《微生物学通报》 CAS CSCD 北大核心 2013年第2期220-227,共8页 Microbiology China
基金 现代农业产业技术体系建设专项资金项目(No.CARS-20-4-4)
关键词 纤维素降解真菌 内切葡聚糖酶活 草酸青霉 Cellulose degrading fungi, CMCase activity, Penicillium oxalicum
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  • 1Tangnu SK,Blanch HW,Wilke CR. Enhanced production of cellulose,hemicellulase and β-xylosidase by Trichoderma reesei (RUT-C30)[J].Biotechnology and Bioengineering,1981,(08):1837-1849.
  • 2张继泉,王瑞明,孙玉英.利用木质纤维素生产燃料酒精的研究进展[J].酿酒科技,2003(1):39-42. 被引量:61
  • 3Lynd LR,Weimer PJ,van Zyl WH. Microbial cellulose utilization:fundamentals and biotechnology[J].Microbiology Molecular Biology Reviews,2002,(03):506-577.doi:10.1128/MMBR.66.3.506-577.2002.
  • 4Verena S,Christian G,Irina SD. The H-yp Creajecorina (Trichoderma reesei) hypercellulolytic mutant RUT C30 lacks a 85kb (29 gene-encoding)region of the wild-type genome[J].BMC Genetics,2008.327.
  • 5宫玉胜,李玉成,吴旺宝,刘珊垚,刘恒.中温(37℃)纤维素分解菌的筛选及混合培养研究[J].生物技术,2010,20(2):50-53. 被引量:14
  • 6Coward-Kelly G,Aiello-Mazzari C,Kim S. Suggested improvements to the standard filter paper assay used to measure cellulase activity[J].Biotechnology and Bioengineering,2003,(06):745-749.
  • 7Mandels M,Sternbrg D. Recent advances in cellulose technology[J].Journal of Fermentation and Technology,1976,(04):267-286.
  • 8Christakopoulos P,Goodenough PW,Kekos D. Purification and characterization of an extracellular β-glucosidase with transglycosylation and exo-glucosidaseactivites from Fusarium oxysporum[J].European Journal of Biochemistry,1994,(02):378-385.
  • 9Li RQ,Wang AY,Kong LD. Isolation and screening of a cellulose-decomposing fungus strain[J].Journal of Shanxi University:Natural Science Edition,2006,(03):317-320.
  • 10魏景超.真菌鉴定手册[M]上海:上海科学技术出版社,1979.

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