Poole R K, Williams H D, Downie J A, Gibson F
Microbial Physiology Research Group, Biosphere Sciences Division, King's College London, UK.
J Gen Microbiol. 1989 Jul;135(7):1865-74. doi: 10.1099/00221287-135-7-1865.
A mutant of Escherichia coli K12 has been isolated affected in a gene, designated cydD, distinct from the three previously described loci involved in the synthesis of assembly of the cytochrome bd oxidase complex. The mutant, obtained by nitrosoguanidine mutagenesis, lacks the spectroscopically detectable components of this oxidase, namely cytochromes b558, b595 and d. Cytochrome oxidase o is the sole CO-binding cytochrome in membranes of the mutant, but the soluble haemoprotein b-590 and catalase activity appear unaffected. Discrimination between Cyd+ and Cyd- strains is facilitated by the development of a defined low-phosphate medium that allows the inclusion of Zn2+ as well as azide, inhibitors of respiratory electron transfer particularly via cytochrome o. Mapping with F-prime factors and by P1 cotransductional frequencies shows the mutation to map near 19.3 min on the E. coli chromosome, distinct from cydC, which maps at 18.9 min. The gene order in this region was tested in a three-factor cross and demonstrates the order zbj::Tn10(YYC199)-cydD-aroA, consistent with cotransduction frequencies.
已分离出大肠杆菌K12的一个突变体,该突变体中一个名为cydD的基因发生了变化,与先前描述的参与细胞色素bd氧化酶复合体合成组装的三个基因座不同。通过亚硝基胍诱变获得的该突变体缺乏这种氧化酶的可通过光谱检测到的成分,即细胞色素b558、b595和d。细胞色素氧化酶o是突变体膜中唯一能与一氧化碳结合的细胞色素,但可溶性血红蛋白b - 590和过氧化氢酶活性似乎未受影响。通过开发一种特定的低磷酸盐培养基来区分Cyd +和Cyd -菌株变得容易,该培养基允许加入锌离子以及叠氮化物,叠氮化物是呼吸电子传递的抑制剂,特别是通过细胞色素o的电子传递。用F - 附加因子和P1共转导频率进行定位表明,该突变位于大肠杆菌染色体上19.3分钟附近,与位于18.9分钟处的cydC不同。在三因子杂交中测试了该区域的基因顺序,结果表明顺序为zbj::Tn10(YYC199)-cydD-aroA,这与共转导频率一致。