Jepsen P K, Riise E, Biedermann K, Kristensen P C, Emborg C
Department of Biotechnology, Technical University of Denmark, Lyngby.
Appl Environ Microbiol. 1987 Oct;53(10):2593-6. doi: 10.1128/aem.53.10.2593-2596.1987.
Two high-nuclease-yielding mutants of Serratia marcescens, derived by chemical mutagenesis (W280, W355), and two strains with the pBR322 plasmid 403-SD2, carrying a nuclease gene and a chloramphenicol resistance gene [Escherichia coli CSH50(403-SD2) and S. marcescens CH30(403-SD2)] were investigated for nuclease production in a factorial shake flask experiment, with temperature (30 and 37 degrees C), pH (with or without CaCO3 tablets), and aeration (with or without baffles) as variable conditions. Yields varied 10-fold depending on the conditions investigated.
通过化学诱变获得的两株高产核酸酶的粘质沙雷氏菌突变体(W280、W355),以及两株携带核酸酶基因和氯霉素抗性基因的pBR322质粒403-SD2菌株[大肠杆菌CSH50(403-SD2)和粘质沙雷氏菌CH30(403-SD2)],在析因摇瓶实验中研究了核酸酶的产生情况,实验将温度(30和37摄氏度)、pH值(添加或不添加碳酸钙片)和通气情况(有或没有挡板)作为可变条件。根据所研究的条件不同,产量变化了10倍。