Xu Zhi-nan, Shen Wen-he, Chen Xi-yang, Lin Jian-ping, Cen Pei-lin
Institute of Bioengineering, Department of Chemical Engineering and Bioengineering, Zhejiang University, 310027, Hangzhou, China.
Biotechnol Lett. 2005 Aug;27(15):1135-40. doi: 10.1007/s10529-005-8463-y.
A novel high-throughput cultivation method was developed to rapidly screen large numbers of rapamycin-producing mutants of Streptomyces hygroscopicus by duplicate culturing of isolates on the surfaces of agar-solidified 96 wells in microtiter plates. One copy of the cultures was used for the rapamycin bioassay and the other identical copy, representing potentially high yielding strains, was preserved for further study. By integrating 96-well solid cultivation and the bioassay, we screened more than 7000 isolates and found 10 high-yielding strains. From these, one mutant produced 420 mug rapamycin/ml, which was double the yield of parent strain used in the submerged fermentation process.
开发了一种新型高通量培养方法,通过在微量滴定板中琼脂固化的96孔表面对分离株进行重复培养,快速筛选大量产雷帕霉素的吸水链霉菌突变体。一份培养物用于雷帕霉素生物测定,另一份相同的培养物代表潜在的高产菌株,用于进一步研究。通过整合96孔固体培养和生物测定,我们筛选了7000多个分离株,发现了10个高产菌株。其中,一个突变体产生420微克雷帕霉素/毫升,是深层发酵过程中使用的亲本菌株产量的两倍。