Xu Hui, Kahlich Rainer, Kammerer Bernd, Heide Lutz, Li Shu-Ming
Pharmazeutische Biologie, Pharmazeutisches Institut, Eberhard-Karls-Universität Tübingen, Auf der Morgenstelle 8, 72076 Tübingen, Germany.
Institut für Pharmakologie und Toxikologie, Abteilung Klinische Pharmakologie, Eberhard-Karls-Universität Tübingen, Otfried-Müller Str. 45, 72076 Tübingen, Germany.
Microbiology (Reading). 2003 Aug;149(Pt 8):2183-2191. doi: 10.1099/mic.0.26314-0.
The aminocoumarin antibiotic clorobiocin contains a 5-methylpyrrole-2-carboxylic acid unit, attached via an ester bond to the 3-OH group of the deoxysugar moiety. To investigate candidate genes responsible for the formation of this ester bond, a gene inactivation experiment was carried out in the clorobiocin producer Streptomyces roseochromogenes var. oscitans DS 12.976. An in-frame deletion was created in the coding sequence of the gene cloN2. The production of secondary metabolites in the wild-type and in the cloN2 mutant was analysed. The wild-type showed clorobiocin as the main product, whereas the cloN2 mutant accumulated a new aminocoumarin derivative, novclobiocin 104, lacking the pyrrole moiety at the 3-OH of the deoxysugar. In addition, free pyrrole-2-carboxylic acid accumulated in the culture extract of the cloN2 mutant. The structures of the metabolites were confirmed by NMR and LC-MS analysis. Clorobiocin production was successfully restored in the cloN2 mutant by introducing a replicative plasmid containing the cloN2 sequence. These results prove an involvement of cloN2 in the formation of the ester bond between the pyrrole moiety and the deoxysugar in clorobiocin biosynthesis. Furthermore, they indicate that the C-methylation at position 5 of the pyrrole moiety occurs after the attachment of pyrrole-2-carboxylic acid unit to the deoxysugar moiety.
氨基香豆素类抗生素氯新生霉素含有一个5-甲基吡咯-2-羧酸单元,该单元通过酯键连接到脱氧糖部分的3-OH基团上。为了研究负责形成这种酯键的候选基因,在氯新生霉素产生菌玫瑰色链霉菌变株迟钝链霉菌DS 12.976中进行了基因失活实验。在基因cloN2的编码序列中产生了一个框内缺失。分析了野生型和cloN2突变体中次生代谢产物的产生情况。野生型以氯新生霉素为主要产物,而cloN2突变体积累了一种新的氨基香豆素衍生物新氯新生霉素104,其在脱氧糖的3-OH处缺少吡咯部分。此外,游离的吡咯-2-羧酸在cloN2突变体的培养提取物中积累。通过核磁共振(NMR)和液相色谱-质谱(LC-MS)分析确定了代谢产物的结构。通过引入含有cloN2序列的复制质粒,成功地在cloN2突变体中恢复了氯新生霉素的产生。这些结果证明cloN2参与了氯新生霉素生物合成中吡咯部分与脱氧糖之间酯键的形成。此外,它们表明吡咯部分5位的C-甲基化发生在吡咯-2-羧酸单元连接到脱氧糖部分之后。