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The Unique tuf2 Gene from the Kirromycin Producer Streptomyces ramocissimus Encodes a Minor and Kirromycin-Sensitive Elongation Factor Tu

机译:来自基罗霉素生产者链霉菌链霉菌的独特tuf2基因编码一个较小的基洛霉素敏感性延伸因子Tu

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摘要

Streptomyces ramocissimus, the producer of elongation factor Tu (EF-Tu)-targeted antibiotic kirromycin, contains three divergent tuf-like genes, with tuf1 encoding regular kirromycin-sensitive EF-Tu1; the functions of tuf2 and tuf3 are unknown. Analysis of the tuf gene organization in nine producers of kirromycin-type antibiotics revealed that they all contain homologues of tuf1 and sometimes of tuf3 but that tuf2 was found in S. ramocissimus only. The tuf2-flanking regions were sequenced, and the two tuf2-surrounding open reading frames were shown to be oriented in opposite directions. In vivo transcription analysis of the tuf2 gene displayed an upstream region with bidirectional promoter activity. The transcription start site of tuf2 was located approximately 290 nucleotides upstream of the coding sequence. Very small amounts of tuf2 transcripts were detected in both liquid- and surface-grown cultures of S. ramocissimus, consistent with the apparent absence of EF-Tu2 in total protein extracts. The tuf2 transcript level was not influenced by the addition of kirromycin to exponentially growing cultures. To assess the function of S. ramocissimus EF-Tu2, the protein was overexpressed in Streptomyces coelicolor LT2. This strain is a J1501 derivative containing His6-tagged EF-Tu1 as the sole EF-Tu species, which facilitated the separation of EF-Tu2 from the interfering EF-Tu1. S. ramocissimus EF-Tu1 and EF-Tu2 were indistinguishable in their ability to stimulate protein synthesis in vitro and exhibited the same kirromycin sensitivity, which excludes the possibility that EF-Tu2 is directly involved in the kirromycin resistance mechanism of S. ramocissimus.
机译:以延伸因子Tu(EF-Tu)为目标的抗生素奇异霉素的生产者,链霉菌(Streptomyces ramocissimus)包含三个不同的tuf样基因,其中tuf1编码常规对奇异霉素敏感的EF-Tu1。 tuf2和tuf3的功能未知。对九种基洛霉素类抗生素生产者中的tuf基因组织进行分析后发现,它们都含有tuf1,有时也包含tuf3的同源物,但tuf2仅在拉美链球菌中发现。对tuf2侧翼区域进行了测序,并显示了两个围绕tuf2的开放阅读框的方向相反。 tuf2基因的体内转录分析显示具有双向启动子活性的上游区域。 tuf2的转录起始位点位于编码序列上游约290个核苷酸处。在拉美链球菌的液体和表面生长培养物中均检测到非常少量的tuf2转录物,这与总蛋白提取物中明显不存在EF-Tu2一致。 tuf2转录水平不受指数增长的培养物中添加奇霉素的影响。为了评估S. ramocissimus EF-Tu2的功能,该蛋白在天蓝色链霉菌LT2中过表达。该菌株是一个J1501衍生物,其中包含带有His6标签的EF-Tu1作为唯一的EF-Tu物种,这有助于从干扰EF-Tu1中分离出EF-Tu2。分支链球菌EF-Tu1和EF-Tu2在体外刺激蛋白质合成的能力上没有区别,并且表现出相同的对奇霉素的敏感性,这排除了EF-Tu2直接参与对链球菌对奇洛霉素的耐药机制的可能性。

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