Breeding and identification of novel koji molds with high activity of acid protease by genome recombination between Aspergillus oryzae and Aspergillus niger

被引:39
|
作者
Xu, Defeng [1 ]
Pan, Li [2 ]
Zhao, Haifeng [1 ]
Zhao, Mouming [1 ]
Sun, Jiaxin [2 ]
Liu, Dongmei [2 ]
机构
[1] S China Univ Technol, Coll Light Ind & Food Sci, Guangzhou 510640, Peoples R China
[2] S China Univ Technol, Sch Biol Sci & Engn, Guangzhou 510006, Guangdong, Peoples R China
关键词
Aspergillus; Genome recombination; Acid protease; Identification; SOLID-STATE-FERMENTATION; ENCODING GENE PEPA; PROTOPLAST FUSION; TRICHODERMA-HARZIANUM; PARENTAL PROTOPLASTS; LACTOCOCCUS-LACTIS; ALKALINE PROTEASE; NICOTIANA-TABACUM; EXPRESSION; GENERATION;
D O I
10.1007/s10295-010-0904-5
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Acid protease is essential for degradation of proteins during soy sauce fermentation. To breed more suitable koji molds with high activity of acid protease, interspecific genome recombination between A. oryzae and A. niger was performed. Through stabilization with d-camphor and haploidization with benomyl, several stable fusants with higher activity of acid protease were obtained, showing different degrees of improvement in acid protease activity compared with the parental strain A. oryzae. In addition, analyses of mycelial morphology, expression profiles of extracellular proteins, esterase isoenzyme profiles, and random amplified polymorphic DNA (RAPD) were applied to identify the fusants through their phenotypic and genetic relationships. Morphology analysis of the mycelial shape of fusants indicated a phenotype intermediate between A. oryzae and A. niger. The profiles of extracellular proteins and esterase isoenzyme electrophoresis showed the occurrence of genome recombination during or after protoplast fusion. The dendrogram constructed from RAPD data revealed great heterogeneity, and genetic dissimilarity indices showed there were considerable differences between the fusants and their parental strains. This investigation suggests that genome recombination is a powerful tool for improvement of food-grade industrial strains. Furthermore, the presented strain improvement procedure will be applicable for widespread use for other industrial strains.
引用
收藏
页码:1255 / 1265
页数:11
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