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Intracellular Butyryl Phosphate and Acetyl Phosphate Concentrations in Clostridium acetobutylicum and Their Implications for Solvent Formation

机译:丙酮丁醇梭菌中细胞内磷酸正丁酯和乙酰磷酸的浓度及其对溶剂形成的影响

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It has been suggested (L. H. Harris, R. P. Desai, N. E. Welker, and E. T. Papoutsakis, Biotechnol. Bioeng. 67:1-11, 2000) that butyryl phosphate (BuP) is a regulator of solventogenesis in Clostridium acetobutylicum. Here, we determined BuP and acetyl phosphate (AcP) levels in fermentations of C. acetobutylicum wild type (WT), degenerate strain M5, a butyrate kinase (buk) mutant, and a phosphotransacetylase (pta) mutant. A sensitive method was developed to measure BuP and AcP in the same sample. Compared to the WT, the buk mutant had higher levels of BuP and AcP; the BuP levels were high during the early exponential phase, and there was a peak corresponding to solvent production. Consistent with this, solvent formation was initiated significantly earlier and was much stronger in the buk mutant than in all other strains. For all strains, initiation of butanol formation corresponded to a BuP peak concentration that was more than 60 to 70 pmol/g (dry weight), and higher and sustained levels corresponded to higher butanol formation fluxes. The BuP levels never exceeded 40 to 50 pmol/g (dry weight) in strain M5, which produces no solvents. The BuP profiles were bimodal, and there was a second peak midway through solventogenesis that corresponded to carboxylic acid reutilization. AcP showed a delayed single peak during late solventogenesis corresponding to acetate reutilization. As expected, in the pta mutant the AcP levels were very low, yet this strain exhibited strong butanol production. These data suggest that BuP is a regulatory molecule that may act as a phosphodonor of transcriptional factors. DNA array-based transcriptional analysis of the buk and M5 mutants demonstrated that high BuP levels corresponded to downregulation of flagellar genes and upregulation of solvent formation and stress genes.
机译:已经提出(L.H.Harris,R.P.Desai,N.E.Welker和E.T.Papoutsakis,Biotechnol.Bioeng.67:1-11,2000),磷酸丁酯(BuP)是丙酮丁醇梭菌中溶剂发生的调节剂。在这里,我们确定了丙酮丁醇梭菌野生型(WT),简并品系M5,丁酸激酶(buk)突变体和磷酸转乙酰酶(pta)突变体发酵中的BuP和乙酰磷酸(AcP)水平。开发了一种灵敏的方法来测量同一样品中的BuP和AcP。与野生型相比,buk突变体的BuP和AcP含量更高;在早期指数阶段,BuP含量很高,并且有一个对应于溶剂产生的峰。与此相一致,在buk突变体中,溶剂形成的开始时间要早得多,并且比所有其他菌株都要强得多。对于所有菌株,丁醇形成的起始对应于高于60至70 pmol / g(干重)的BuP峰值浓度,较高和持续的水平对应于较高的丁醇形成通量。在不产生溶剂的菌株M5中,BuP的水平从未超过40至50 pmol / g(干重)。 BuP曲线是双峰的,并且在溶剂生成过程中出现了第二个峰,对应于羧酸的再利用。 AcP在后期溶剂生成过程中显示出延迟的单峰,对应于乙酸盐的再利用。正如预期的那样,在pta突变体中,AcP水平非常低,但是该菌株表现出较强的丁醇产量。这些数据表明,BuP是一种调节性分子,可以充当转录因子的磷酸化供体。基于DNA阵列的buk和M5突变体的转录分析表明,高BuP含量对应于鞭毛基因的下调以及溶剂形成和应激基因的上调。

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