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首页> 外文期刊>Journal of bacteriology >Induction of actinorhodin production by rpsL (encoding ribosomal protein S12) mutations that confer streptomycin resistance in Streptomyces lividans and Streptomyces coelicolor A3(2).
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Induction of actinorhodin production by rpsL (encoding ribosomal protein S12) mutations that confer streptomycin resistance in Streptomyces lividans and Streptomyces coelicolor A3(2).

机译:rpsL(编码核糖体蛋白S12)突变诱导放线菌丝蛋白的产生,该突变赋予lividans链霉菌和coelicolor链霉菌A3中的链霉素抗性(2)。

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A strain of Streptomyces lividans, TK24, was found to produce a pigmented antibiotic, actinorhodin, although S. lividans normally does not produce this antibiotic. Genetic analyses revealed that a streptomycin-resistant mutation str-6 in strain TK24 is responsible for induction of antibiotic synthesis. DNA sequencing showed that str-6 is a point mutation in the rpsL gene encoding ribosomal protein S12, changing Lys-88 to Glu. Gene replacement experiments with the Lys88-->Glu str allele demonstrated unambiguously that the str mutation is alone responsible for the activation of actinorhodin production observed. In contrast, the strA1 mutation, a genetic marker frequently used for crosses, did not restore actinorhodin production and was found to result in an amino acid alteration of Lys-43 to Asn. Induction of actinorhodin production was also detected in strain TK21, which does not harbor the str-6 mutation, when cells were incubated with sufficient streptomycin or tetracycline to reduce the cell's growth rate, and 40 and 3% of streptomycin- or tetracycline-resistant mutants, respectively, derived from strain TK21 produced actinorhodin. Streptomycin-resistant mutations also blocked the inhibitory effects of relA and brgA mutations on antibiotic production, aerial mycelium formation or both. These str mutations changed Lys-88 to Glu or Arg and Arg-86 to His in ribosomal protein S12. The decrease in streptomycin production in relC mutants in Streptomyces griseus could also be abolished completely by introducing streptomycin-resistant mutations, although the impairment in antibiotic production due to bldA (in Streptomyces coelicolor) or afs mutations (in S. griseus) was not eliminated. These results indicate that the onset and extent of secondary metabolism in Streptomyces spp. is significantly controlled by the translational machinery.
机译:尽管青紫链霉菌通常不产生这种抗生素,但发现青紫链霉菌菌株TK24产生有色的抗生素放线菌素。遗传分析表明,TK24菌株中链霉素抗性突变str-6负责诱导抗生素合成。 DNA测序表明,str-6是编码核糖体蛋白S12的rpsL基因中的一个点突变,将Lys-88变为Glu。用Lys88-> Glu str等位基因进行的基因替换实验清楚地表明,str突变是导致所观察到的放线菌素生成激活的唯一原因。相反,strA1突变是一种经常用于杂交的遗传标记,不能恢复放线菌丝蛋白的产生,并发现其导致Lys-43的氨基酸改变为Asn。当将细胞与足够的链霉素或四环素一起孵育以降低细胞的生长速率以及40%和3%的抗链霉素或四环素的突变体孵育时,在不具有str-6突变的TK21菌株中也检测到肌动球蛋白的诱导。分别来自菌株TK21产生的放线菌丝蛋白。链霉素抗性突变也阻断了relA和brgA突变对抗生素产生,气生菌丝形成或两者的抑制作用。这些str突变使核糖体蛋白S12中的Lys-88变为Glu或Arg,而Arg-86变为His。尽管并未消除由于bldA(链霉菌中的色氨酸)或afs突变(灰霉菌)引起的抗生素生产的损害,但也可以通过引入抗链霉素的突变完全消除灰链霉菌中relC突变体链霉素产生的减少。这些结果表明链霉菌属中次生代谢的发生和程度。受到翻译机的明显控制。

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