摘要
目的:通过了解高产果胶酶菌株EIM-4的背景信息及优化其最适的产酶条件,为下一步工业化生产提供依据。方法:通过基于18S rDNA序列的系统发育进化分析对果胶酶高产菌进行鉴定,通过单因素试验和均匀设计获得最适产酶条件。结果:通过对18SrRNA基因的分子系统进化分析,菌株EIM-4被鉴定为黑曲霉(Aspergillus niger)。通过单因素和均匀设计试验确定最佳产酶培养基为(g/L):橘皮粉32.9,黄豆粉10.7,(NH4)SO42.1,CaCO31.0,pH自然。结论:Aspergillus niger EIM-4的液体发酵产果胶酶的活力可达15159.82U/mL。
Objective:Developing available industrial technologies to produce pectinase by understanding basic information for a high pecfinaseproducing strain EIM4 and optimizing its submerged fermentation conditions. Method: Identified strain EIM4 by using molecular phyloganatic analysis of 18S rDNA sequences and improved pectinase production by orthogonal experiment design. Result:Strain ElM- 4 was identified as Aspergillus ruiger. Through orthogonal experiment, the optimal submerge fermentation condition was obtained for producing extracellular pectinase. suitable medium contained: orange peel power 32.97g/L, soybean flour 10.76g/L, (NIL)SO4 2.14g/L, CaCO3 1.00g/L., nature pH. Condusion:The optimum pectinase activity of Aspergillus niger EIM-4 is as high as 15 159.82U/ml.
出处
《生物技术》
CAS
CSCD
2008年第5期69-72,共4页
Biotechnology
基金
福建省科技厅重大项目(2005Q007)资助
关键词
果胶酶
黑曲霉
分子系统进化
液体发酵
均匀设计
pectinase
Aspergillus niger
phylogenetic analysis
submerge fermentation
orthogonal experiment