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lanI在蓝霉素链霉菌S136中对landomycin A生物合成的调控功能以及与编码链霉菌抗生素调控蛋白的基因的交叉互补研究。

Function of lanI in regulation of landomycin A biosynthesis in Streptomyces cyanogenus S136 and cross-complementation studies with Streptomyces antibiotic regulatory proteins encoding genes.

作者信息

Rebets Yuriy, Dutko Lilia, Ostash Bohdan, Luzhetskyy Andriy, Kulachkovskyy Olexandr, Yamaguchi Toshio, Nakamura Tatsunosuke, Bechthold Andreas, Fedorenko Victor

机构信息

Department of Genetics and Biotechnology of Ivan Franko National University of L'viv, Grushevskogo st.4, L'viv, 79005, Ukraine.

出版信息

Arch Microbiol. 2008 Feb;189(2):111-20. doi: 10.1007/s00203-007-0299-5. Epub 2007 Sep 5.

Abstract

The transcriptional regulator of landomycin A biosynthesis encoded by lanI gene has been inactivated within the chromosome of Streptomyces cyanogenus S136. The obtained mutant strain did not produce landomycin A and its known intermediates. Loss of landomycin A production caused significant changes in morphology of the lanI deficient strain. RT-PCR analysis confirmed complete cessation of transcription of certain lan genes, including lanJ (encoding putative proton dependent transporter) and lanK (presumably involved in lanJ expression regulation). Introduction of either lanI or lndI [lanI homologue controlling landomycin E biosynthesis in Streptomyces globisporus 1912, both encoding Streptomyces antibiotic regulatory proteins (SARPs)] restored landomycin A production in the mutant strain. Chimeric constructs ladI and ladR were generated by exchanging the DNA sequences corresponding to N- and C-terminal parts of LndI and LanI. None of these genes were able to activate the production of landomycins in regulatory mutants of S. cyanogenus and S. globisporus. Nevertheless, the production of novel unidentified compound was observed in the case of S. cyanogenus harboring ladI gene. Various genes encoding SARPs have been expressed in S. globisporus and S. cyanogenus regulatory mutants and the results of these complementation experiments are discussed.

摘要

由lanI基因编码的地霉素A生物合成转录调节因子已在产蓝链霉菌S136的染色体中失活。获得的突变菌株不产生地霉素A及其已知中间体。地霉素A产量的丧失导致lanI缺陷菌株的形态发生显著变化。RT-PCR分析证实某些lan基因的转录完全停止,包括lanJ(编码假定的质子依赖性转运蛋白)和lanK(可能参与lanJ表达调控)。引入lanI或lndI [在球形链霉菌1912中控制地霉素E生物合成的lanI同源物,两者都编码链霉菌抗生素调节蛋白(SARPs)]可恢复突变菌株中地霉素A的产量。通过交换对应于LndI和LanI的N端和C端部分的DNA序列产生嵌合构建体ladI和ladR。这些基因均不能激活产蓝链霉菌和球形链霉菌调节突变体中地霉素的产生。然而,在携带ladI基因的产蓝链霉菌中观察到了新型未知化合物的产生。已在球形链霉菌和产蓝链霉菌调节突变体中表达了各种编码SARPs的基因,并讨论了这些互补实验的结果。

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