Dutko Lilia, Rebets Yuriy, Ostash Bohdan, Luzhetskyy Andriy, Bechthold Andreas, Nakamura Tatsunosuke, Fedorenko Victor
Department of Genetics and Biotechnology of Ivan Franko National University of L'viv, L'viv, Ukraine.
FEMS Microbiol Lett. 2006 Feb;255(2):280-5. doi: 10.1111/j.1574-6968.2005.00085.x.
The prx gene, which is highly homologous to putative proteinases, has been identified by sequencing in the vicinity of the biosynthetic gene cluster for landomycin E (LaE) biosynthesis (lnd) in Streptomyces globisporus 1912. The S. globisporus Pro6 gene, deficient in prx, produced fivefold less LaE than the parental strain. The expression of prx in S. globisporus Pro6 restored LaE production to wild-type levels, whereas expression of the pathway-specific regulatory gene lndI did not. The introduction of additional copies of prx into the wild-type strain using a pSG5-based plasmid, pKC1139, led to a 2.7-fold increase in LaE production. These results indicate that prx is a novel regulatory gene for LaE biosynthesis.
prx基因与假定的蛋白酶高度同源,通过对球孢链霉菌1912中landomycin E(LaE)生物合成(lnd)的生物合成基因簇附近进行测序得以鉴定。缺乏prx的球孢链霉菌Pro6基因产生的LaE比亲本菌株少五倍。prx在球孢链霉菌Pro6中的表达将LaE产量恢复到野生型水平,而途径特异性调节基因lndI的表达则没有。使用基于pSG5的质粒pKC1139将额外的prx拷贝引入野生型菌株,导致LaE产量增加2.7倍。这些结果表明prx是LaE生物合成的一个新的调节基因。