Alijah R, Dorendorf J, Talay S, Pühler A, Wohlleben W
Universität Bielefeld, Lehrstuhl für Genetik, Federal Republic of Germany.
Appl Microbiol Biotechnol. 1991 Mar;34(6):749-55. doi: 10.1007/BF00169345.
Streptomyces viridochromogenes Tü494 produces the antibiotic phosphinothricyl-alanyl-alanine (Ptt). Ptt-non-producing mutants were isolated following N-methyl-N'-nitro-N-nitrosoguanidine (NTG) or UV light treatment of spore suspensions. In co-synthesis and bioconversion experiments the mutational blocks in the biosynthetic pathway were localized. The mutant NTG1 was analysed in detail. This mutant acts as a secretor for all other mutants. From bioconversion experiments with presumptive precursors circumstantial evidence was obtained that NTG1 is mutated in a gene involved in the alanylation of N-acetyl-demethyl-phosphinothricin. Using a cosmid gene library the DNA region complementing the defective gene of mutant NTG1 was isolated on a 4-kb BamHI fragment. Subcloning experiments showed that a 3-kb BglII/BamHI fragment is sufficient for complementation of mutant NTG1.
绿色产色链霉菌Tü494产生抗生素膦丝菌素 - 丙氨酰 - 丙氨酸(Ptt)。在用N - 甲基 - N'-硝基 - N - 亚硝基胍(NTG)或紫外线处理孢子悬液后,分离出不产生Ptt的突变体。在共合成和生物转化实验中,确定了生物合成途径中的突变位点。对突变体NTG1进行了详细分析。该突变体对所有其他突变体起到分泌作用。通过对推测前体的生物转化实验,间接证据表明NTG1在一个参与N - 乙酰 - 去甲基 - 膦丝菌素丙氨酰化的基因中发生了突变。利用黏粒基因文库,在一个4kb的BamHI片段上分离出了与突变体NTG1缺陷基因互补的DNA区域。亚克隆实验表明,一个3kb的BglII / BamHI片段足以使突变体NTG1互补。