Tang Gong-Li, Cheng Yi-Qiang, Shen Ben
Division of Pharmaceutical Sciences, University of Wisconsin, Madison, Wisconsin 53705, USA.
Chem Biol. 2004 Jan;11(1):33-45. doi: 10.1016/j.chembiol.2003.12.014.
A 135,638 bp DNA region that encompasses the leinamycin (LNM) biosynthetic gene cluster was sequenced from Streptomyces atroolivaceus S-140. The boundaries of the lnm cluster were defined by systematic inactivation of open reading frames within the sequenced region. The lnm cluster spans 61.3 kb of DNA and consists of 27 genes encoding nonribosomal peptide synthetase (NRPS), polyketide synthase (PKS), hybrid NRPS-PKS, resistance, regulatory, and tailoring enzymes, as well as proteins of unknown function. A model for LNM biosynthesis is proposed, central to which is the LNM hybrid NRPS-PKS megasynthetase consisting of discrete (LnmQ and LnmP) and modular (LnmI) NRPS, acyltransferase-less PKS (LnmG, LnmI, and LnmJ), and PKS modules with unusual domain organization. These studies unveil an unprecedented architectural complexity for the LNM hybrid NRPS-PKS megasynthetase and set the stage to investigate the molecular basis for LNM biosynthesis.
从橄榄色链霉菌S-140中测序了一个包含链黑霉素(LNM)生物合成基因簇的135,638 bp DNA区域。通过对测序区域内开放阅读框的系统失活来确定lnm簇的边界。lnm簇跨越61.3 kb的DNA,由27个基因组成,这些基因编码非核糖体肽合成酶(NRPS)、聚酮合酶(PKS)、杂合NRPS-PKS、抗性、调节和修饰酶,以及功能未知的蛋白质。提出了一个LNM生物合成模型,其核心是由离散的(LnmQ和LnmP)和模块化的(LnmI)NRPS、无酰基转移酶的PKS(LnmG、LnmI和LnmJ)以及具有异常结构域组织的PKS模块组成的LNM杂合NRPS-PKS巨型合成酶。这些研究揭示了LNM杂合NRPS-PKS巨型合成酶前所未有的结构复杂性,并为研究LNM生物合成的分子基础奠定了基础。