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产漆酶菌株筛选及一株产酶菌株的优化与鉴定
引用本文:张延威,邱树毅,韩燕峰,梁宗琦.产漆酶菌株筛选及一株产酶菌株的优化与鉴定[J].微生物学通报,2014,41(2):251-257.
作者姓名:张延威  邱树毅  韩燕峰  梁宗琦
作者单位:1. 贵州大学 生命科学学院 贵州 贵阳 550025; 2. 贵州师范学院 贵州省生物资源开发利用特色重点实验室 贵州 贵阳 550018;1. 贵州大学 生命科学学院 贵州 贵阳 550025;1. 贵州大学 生命科学学院 贵州 贵阳 550025;1. 贵州大学 生命科学学院 贵州 贵阳 550025
基金项目:贵州省优秀青年科技人才培养对象专项资金项目(No. 黔科合人字(2013)05号)
摘    要:【目的】从26株真菌菌株中筛选高产漆酶菌株。【方法】采用愈创木酚法进行产漆酶菌株的筛选,通过正交实验对筛选出的高产菌株进行优化,并通过形态学和分子系统学对菌株进行鉴定。【结果】26株真菌菌株中有4株可产生漆酶,其中菌株H52.1为产漆酶最好菌株;菌株H52.1产漆酶优化培养基碳源为可溶性淀粉,氮源为硝酸铵,pH为8,金属离子为Ca2+;经鉴定,该菌株为大孢戴氏霉。【结论】大孢戴氏霉在产漆酶方面值得进一步研究开发。

关 键 词:漆酶,优化,戴氏霉,大孢戴氏霉

Screening of fungal strains with laccase and optimization and identification of the strain with high-yield laccase
ZHANG Yan-Wei,QIU Shu-Yi,HAN Yan-Feng and LIANG Zong-Qi.Screening of fungal strains with laccase and optimization and identification of the strain with high-yield laccase[J].Microbiology,2014,41(2):251-257.
Authors:ZHANG Yan-Wei  QIU Shu-Yi  HAN Yan-Feng and LIANG Zong-Qi
Affiliation:1. College of Life Sciences, Guizhou University, Guiyang, Guizhou 550025, China; 2. Key Laboratory of Guizhou Bioresource Development and Utilization, Guizhou Normal College, Guiyang, Guizhou 550018, China;1. College of Life Sciences, Guizhou University, Guiyang, Guizhou 550025, China;1. College of Life Sciences, Guizhou University, Guiyang, Guizhou 550025, China;1. College of Life Sciences, Guizhou University, Guiyang, Guizhou 550025, China
Abstract:Objective] To obtain the fungal stain with high-yield laccase. Methods] Strains producing laccase were screened out by the guaiacol method. Then the strain with the high-yield laccase screened was optimized by the orthogonal experiment design and identified using the morphological characters and the molecular systematics. Results] Four strains could produce laccase in these 26 fungal strains, and the strain H52.1 was the best high-yield strain, and its optimal medium components and conditions were as follows, the optimal carbon source was soluble starch, nitrogen source was ammonium nitrate, pH value was 8 and metal ion was Ca2+. The result of identification showed that the strain H52.1 was Taifanglania major. Conclusion] Taifanglania major has been worth doing further research and exploitation in the laccase development.
Keywords:Laccase  Optimization  Taifanglania  Taifanglania major
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