Sekurova Olga N, Brautaset Trygve, Sletta Håvard, Borgos Sven E F, Jakobsen M Øyvind M, Ellingsen Trond E, Strøm Arne R, Valla Svein, Zotchev Sergey B
Department of Biotechnology, Norwegian University of Science and Technology, N-7491 Trondheim. SINTEF Industrial Biotechnology, SINTEF, N-7034 Trondheim, Norway.
J Bacteriol. 2004 Mar;186(5):1345-54. doi: 10.1128/JB.186.5.1345-1354.2004.
Six putative regulatory genes are located at the flank of the nystatin biosynthetic gene cluster in Streptomyces noursei ATCC 11455. Gene inactivation and complementation experiments revealed that nysRI, nysRII, nysRIII, and nysRIV are necessary for efficient nystatin production, whereas no significant roles could be demonstrated for the other two regulatory genes. To determine the in vivo targets for the NysR regulators, chromosomal integration vectors with the xylE reporter gene under the control of seven putative promoter regions upstream of the nystatin structural and regulatory genes were constructed. Expression analyses of the resulting vectors in the S. noursei wild-type strain and regulatory mutants revealed that the four regulators differentially affect certain promoters. According to these analyses, genes responsible for initiation of nystatin biosynthesis and antibiotic transport were the major targets for regulation. Data from cross-complementation experiments showed that nysR genes could in some cases substitute for each other, suggesting a functional hierarchy of the regulators and implying a cascade-like mechanism of regulation of nystatin biosynthesis.
六个假定的调控基因位于诺尔斯链霉菌ATCC 11455中制霉菌素生物合成基因簇的侧翼。基因失活和互补实验表明,NysRI、NysRII、NysRIII和NysRIV对高效生产制霉菌素是必需的,而另外两个调控基因未显示出显著作用。为了确定NysR调控因子的体内作用靶点,构建了在制霉菌素结构和调控基因上游七个假定启动子区域控制下带有xylE报告基因的染色体整合载体。对所得载体在诺尔斯链霉菌野生型菌株和调控突变体中的表达分析表明,这四个调控因子对某些启动子有不同的影响。根据这些分析,负责制霉菌素生物合成起始和抗生素转运的基因是主要的调控靶点。交叉互补实验的数据表明,NysR基因在某些情况下可以相互替代,这表明调控因子存在功能层次结构,并暗示了制霉菌素生物合成的级联调控机制。