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Acetohydroxy acid synthase I, a required enzyme for isoleucine and valine biosynthesis in Escherichia coli K-12 during growth on acetate as the sole carbon source.

机译:乙酰羟酸合酶I,是在乙酸盐作为唯一碳源生长期间,大肠杆菌K-12中异亮氨酸和缬氨酸生物合成所需的酶。

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摘要

Escherichia coli K-12 has two acetohydroxy acid synthase (AHAS) isozymes (AHAS I and AHAS III). Both of these isozymes catalyze the synthesis of alpha-aceto-alpha-hydroxybutyrate and alpha-acetolactate, which are key intermediates of the isoleucine-valine biosynthetic pathway. Strains lacking either isozyme but not both activities have been previously shown to grow well in minimal media in the absence of isoleucine and valine on any of several commonly used carbon sources (e.g., glucose or succinate). We report the characterization of mutants that were unable to grow on either acetate or oleate as a sole carbon source due to a defect in isoleucine-valine biosynthesis. The defect in isoleucine-valine biosynthesis was expressed only on these carbon sources and was due to the loss of AHAS I activity, resulting from lesions in the ilvBN operon. Previously identified ilvBN mutant strains also failed to grow on acetate or oleate minimal media. Our results indicated that AHAS I is an essential enzyme for isoleucine and valine biosynthesis when E. coli K-12 is grown on acetate or oleate as the sole carbon source. AHAS III was expressed during growth on acetate or oleate but was somehow unable to produce sufficient amounts of alpha-aceto-alpha-hydroxybutyrate and alpha-acetolactate to allow growth.
机译:大肠杆菌K-12具有两个乙酰羟酸合酶(AHAS)同功酶(AHAS I和AHAS III)。这两种同工酶均催化α-乙酰-α-羟基丁酸酯和α-乙酰乳酸的合成,它们是异亮氨酸-缬氨酸生物合成途径的关键中间体。先前已显示,缺乏一种同工酶但没有两种活性的菌株在几种常用碳源(例如葡萄糖或琥珀酸盐)中的任何一种上都没有异亮氨酸和缬氨酸的情况下,在基本培养基中生长良好。我们报告了由于异亮氨酸-缬氨酸生物合成缺陷而无法在乙酸盐或油酸盐上作为唯一碳源生长的突变体的表征。异亮氨酸-缬氨酸生物合成的缺陷仅在这些碳源上表达,并且是由于ilvBN操纵子的损伤导致AHAS I活性降低。先前鉴定的ilvBN突变菌株也无法在乙酸盐或油酸盐基本培养基上生长。我们的结果表明,当大肠杆菌K-12以乙酸或油酸盐作为唯一碳源生长时,AHAS I是异亮氨酸和缬氨酸生物合成的必需酶。 AHAS III在乙酸盐或油酸盐的生长过程中表达,但不知何故无法产生足够量的α-乙酰-α-羟基丁酸酯和α-乙酰乳酸以使其生长。

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  • 作者

    Dailey, F E; Cronan, J E;

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  • 年度 1986
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  • 正文语种 en
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