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Global Expression Profiling and Physiological Characterization of Corynebacterium glutamicum Grown in the Presence of l-Valine

机译:L-缬氨酸存在下生长的谷氨酸棒杆菌的全局表达谱和生理学表征

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Addition of l-valine (50 to 200 mM) to glucose minimal medium had no effect on the growth of wild-type Corynebacterium glutamicum ATCC 13032 but inhibited the growth of the derived valine production strain VAL1 [13032 ΔilvA ΔpanBC(pJC1ilvBNCD)] in a concentration-dependent manner. In order to explore this strain-specific valine effect, genomewide expression profiling was performed using DNA microarrays, which showed that valine caused an increased ilvBN mRNA level in VAL1 but not in the wild type. This unexpected result was confirmed by an increased cellular level of the ilvB protein product, i.e., the large subunit of acetohydroxyacid synthase (AHAS), and by an increased AHAS activity of valine-treated VAL1 cells. The conclusion that valine caused the limitation of another branched-chain amino acid was confirmed by showing that high concentrations of l-isoleucine could relieve the valine effect on VAL1 whereas l-leucine had the same effect as valine. The valine-caused isoleucine limitation was supported by the finding that the inhibitory valine effect was linked to the ilvA deletion that results in isoleucine auxotrophy. Taken together, these results implied that the valine effect is caused by competition for uptake of isoleucine by the carrier BrnQ, which transports all branched-chained amino acids. Indeed, valine inhibition could also be relieved by supplementing VAL1 with the dipeptide isoleucyl-isoleucine, which is taken up by a dipeptide transport system rather than by BrnQ. Interestingly, addition of external valine stimulated valine production by VAL1. This effect is most probably due to a reduced carbon usage for biomass production and to the increased expression of ilvBN, indicating that AHAS activity may still be a limiting factor for valine production in the VAL1 strain.
机译:在葡萄糖基本培养基中添加50到200 mM的缬氨酸对野生型谷氨酸棒杆菌ATCC 13032的生长没有影响,但抑制了衍生的缬氨酸生产菌株VAL1 [13032Δ]的生长 ilvA Δ panBC (pJC1 ilvBNCD )]呈浓度依赖性。为了探索这种菌株特异的缬氨酸作用,使用DNA微阵列进行了全基因组表达谱分析,结果表明缬氨酸引起VAL1中 ilvBN mRNA水平的升高,而在野生型中不升高。出乎意料的结果是通过 ilvB 蛋白产物的细胞水平升高,即乙酰羟酸合酶(AHAS)的大亚基,以及缬氨酸处理的VAL1细胞的AHAS活性升高而得到证实的。通过显示高浓度的L-异亮氨酸可以缓解缬氨酸对VAL1的作用,而L-亮氨酸与缬氨酸具有相同的作用,从而证实了缬氨酸引起另一种支链氨基酸的局限性的结论。缬氨酸引起的异亮氨酸限制作用受到以下发现的支持:抑制性缬氨酸作用与导致异亮氨酸营养缺陷的 ilvA 缺失有关。两者合计,这些结果暗示缬氨酸作用是由运输所有支链氨基酸的载体BrnQ竞争吸收异亮氨酸引起的。确实,缬氨酸抑制作用也可以通过向VAL1中补充二肽异亮氨酰-异亮氨酸来缓解,该二肽异亮氨酸-异亮氨酸由二肽转运系统而非BrnQ吸收。有趣的是,添加外部缬氨酸可刺激VAL1刺激缬氨酸产生。这种作用很可能是由于减少了生物质生产中的碳消耗量以及 ilvBN 的表达增加,表明AHAS活性可能仍然是VAL1菌株中缬氨酸生产的限制因素。

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