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黑曲霉转化系统的优化及重组菌株高效筛选
引用本文:李岑,刘松,堵国成.黑曲霉转化系统的优化及重组菌株高效筛选[J].食品与发酵工业,2022(3):1-8.
作者姓名:李岑  刘松  堵国成
作者单位:粮食发酵工艺与技术国家工程实验室(江南大学);江南大学生物工程学院
基金项目:国家重点研发计划项目(2019YFA0905300);国家自然科学基金项目(31771913);国家自然科学基金项目(32071474)。
摘    要:黑曲霉(Aspergillus niger)是食品工业中重要的生产菌株,广泛应用于酶和有机酸生产.为提高黑曲霉遗传操作效率,对黑曲霉转化及重组菌株筛选策略进行优化.基于已报道的最佳转化条件对黑曲霉AG11进行电转化、农杆菌介导和聚乙二醇(polyethylene glycol,PEG)介导转化(Agrobacteriu...

关 键 词:黑曲霉  PEG介导转化  原生质体  流式细胞仪  绿色荧光蛋白  天冬酰胺酶

Optimization of Aspergillus niger transformation system and efficient screening of recombinant strains
LI Cen,LIU Song,DU Guocheng.Optimization of Aspergillus niger transformation system and efficient screening of recombinant strains[J].Food and Fermentation Industries,2022(3):1-8.
Authors:LI Cen  LIU Song  DU Guocheng
Affiliation:(National Engineering Laboratory for Cereal Fermentation Technology,Jiangnan University,Wuxi 214122,China;School of Biotechnology,Jiangnan University,Wuxi 214122,China)
Abstract:Aspergillus niger is an important production strain in food industry,widely used in production of enzymes and organic acids.To improve the genetic efficiency of A.niger,the transformation and recombinant strain screening strategies were optimized.According to the reported optimal transformation conditions,A.niger AG11 was transformed via electroporation,Agrobacterium-mediated and PEG-mediated transformation(PMT),and a hygromycin transformation plate yield 0,30,and 6 transformants,respectively.PMT achieved the highest positive rate of transformants.Based on the optimized protoplast preparation condition:0.8-1 g loose mycelial pellets were incubated in 10 mL Yatalase solution(0.8 mg/mL,pH 5.5)for 2.5 h to obtain protoplasts and used to PMT,the transformation efficiency was increased by 14-fold than that before optimization.To improve the screening efficiency of transformants,the asparaginase(ASN)gene fused with green fluorescent protein(GFP)was integrated into the glycosylase locus of A.niger AG11,and those spores expressing ASN were sorted by flow cytometry.The results showed that 0.3%of the spores could express the GFP(a total of 300000 spores were screened).Enzyme activity analysis indicated that 65%of the spores expressing GFP could produce ASN.These results provide an important methodological basis for gene editing of A.niger.
Keywords:Aspergillus niger  polyethylene glycol-mediated transformation  protoplast  flow cytometer  green fluorescent protein  asparaginase
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