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Molecular Mechanisms Underlying the Positive Stringent Response of the Bacillus subtilis ilv-leu Operon, Involved in the Biosynthesis of Branched-Chain Amino Acids▿

机译:枯草芽孢杆菌il-leu操纵子积极严格反应的分子机制,涉及支链氨基酸的生物合成▿

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摘要

Branched-chain amino acids are the most abundant amino acids in proteins. The Bacillus subtilis ilv-leu operon is involved in the biosynthesis of branched-chain amino acids. This operon exhibits a RelA-dependent positive stringent response to amino acid starvation. We investigated this positive stringent response upon lysine starvation as well as decoyinine treatment. Deletion analysis involving various lacZ fusions revealed two molecular mechanisms underlying the positive stringent response of ilv-leu, i.e., CodY-dependent and -independent mechanisms. The former is most likely triggered by the decrease in the in vivo concentration of GTP upon lysine starvation, GTP being a corepressor of the CodY protein. So, the GTP decrease derepressed ilv-leu expression through detachment of the CodY protein from its cis elements upstream of the ilv-leu promoter. By means of base substitution and in vitro transcription analyses, the latter (CodY-independent) mechanism was found to comprise the modulation of the transcription initiation frequency, which likely depends on fluctuation of the in vivo RNA polymerase substrate concentrations after stringent treatment, and to involve at least the base species of adenine at the 5′ end of the ilv-leu transcript. As discussed, this mechanism is presumably distinct from that for B. subtilis rrn operons, which involves changes in the in vivo concentration of the initiating GTP.
机译:支链氨基酸是蛋白质中最丰富的氨基酸。枯草芽孢杆菌ilv-leu操纵子参与支链氨基酸的生物合成。该操纵子表现出对氨基酸饥饿的依赖于RelA的阳性严格反应。我们调查了赖氨酸饥饿以及辅嘌呤治疗后这种积极严格的反应。涉及各种lacZ融合的缺失分析揭示了ilv-leu阳性严格应答的两种分子机制,即CodY依赖性和非依赖性机制。前者最有可能是由于赖氨酸饥饿引起的体内GTP浓度降低而触发的,GTP是CodY蛋白的核心抑制剂。因此,GTP的降低是通过CodY蛋白从其在ilv-leu启动子上游的顺式元件分离而使ilv-leu表达降低。通过碱基取代和体外转录分析,发现后者(独立于CodY的)机制包括转录起始频率的调节,这可能取决于严格处理后体内RNA聚合酶底物浓度的波动,以及在ilv-leu转录物的5'端至少涉及腺嘌呤的碱基种类。如所讨论的,该机制可能与枯草芽孢杆菌操纵子的机制不同,后者涉及起始GTP的体内浓度的变化。

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