Asdornnithee S, Akiyama K, Takata R
Department of Biotechnology, College of Agriculture, Ehime University, Japan.
Arch Microbiol. 1994;161(5):414-7. doi: 10.1007/BF00288952.
Serratia marcescens mutants, which excrete Escherichia coli alkaline phosphatase (APase) encoded by the plasmid-bearing phoA gene, were isolated after mutagenesis by N-methyl-N'-nitro-N-nitrosoguanidine. These mutants produced two to four times as much APase as did the parent strain under a phosphate-limiting condition, and more than 70% of the enzyme was released into the culture medium. In addition, overproduction and excretion of beta-lactamase was observed in these mutants.
通过用N-甲基-N'-硝基-N-亚硝基胍诱变后,分离出了粘质沙雷氏菌突变体,这些突变体能分泌由携带phoA基因的质粒编码的大肠杆菌碱性磷酸酶(APase)。在磷酸盐限制条件下,这些突变体产生的APase是亲本菌株的两到四倍,并且超过70%的酶被释放到培养基中。此外,在这些突变体中还观察到β-内酰胺酶的过量产生和分泌。