Beyer S, Distler J, Piepersberg W
Bergische Universität GH Wuppertal, Germany.
Mol Gen Genet. 1996 Apr 10;250(6):775-84. doi: 10.1007/BF02172990.
Two divergently oriented operons, strXU and strVW, located within the gene cluster for 5'-hydroxystreptomycin (5'-OH-Sm) biosynthesis in Streptomyces glaucescens strain GAL.0 (ETH 22794), were analysed by DNA sequencing and transcription/regulation studies. Three genes, strU and strVW, are conserved in a similar arrangement but in a different location within the str/sts gene cluster of the Sm-producing strain S. griseus N2-3-11. The four putative products resemble NDP-4-ketohexose 3,5-epimerases (StrX, M(r) 20.2 kDa), NAD(P)-dependent oxidoreductases (StrU, 45.6 kDa), and ABC-transporters (StrV, 61.8 kDa; StrW, 63.4 kDa). These genes are apparently involved in the biosynthesis of 5'-OH-Sm because the promoters of both operons are activated in trans by the activator StrR of S. griseus N2-3-11, when cloned in S. lividans 66 TK23. A sequence motif resembling the consensus sequence GTTCGActG(N)11CagTcGAAc for binding of StrR was identified within the intergenic region of strX and strV. Specific binding of StrR to this site was demonstrated by gel retardation assays using purified His*Tag-StrR.
对青灰链霉菌菌株GAL.0(ETH 22794)中5'-羟基链霉素(5'-OH-Sm)生物合成基因簇内两个方向相反的操纵子strXU和strVW进行了DNA测序以及转录/调控研究。三个基因,即strU和strVW,在产生链霉素的灰色链霉菌菌株N2-3-11的str/sts基因簇内以相似的排列方式保守存在,但位置不同。这四个推定产物类似于NDP-4-酮己糖3,5-差向异构酶(StrX,分子量20.2 kDa)、NAD(P)依赖性氧化还原酶(StrU,45.6 kDa)以及ABC转运蛋白(StrV,61.8 kDa;StrW,63.4 kDa)。这些基因显然参与了5'-OH-Sm的生物合成,因为当克隆到变铅青链霉菌66 TK23中时,两个操纵子的启动子都被灰色链霉菌N2-3-11的激活剂StrR反式激活。在strX和strV的基因间隔区内鉴定出了一个类似于StrR结合共有序列GTTCGActG(N)11CagTcGAAc的序列基序。使用纯化的His*Tag-StrR通过凝胶阻滞试验证明了StrR与该位点的特异性结合。