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首页> 外文期刊>RSC Advances >Transcriptional regulation of xylose utilization in Enterococcus mundtii QU 25
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Transcriptional regulation of xylose utilization in Enterococcus mundtii QU 25

机译:肠球菌MUNDTII QU 25中木糖利用的转录调节

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摘要

Enterococcus mundtii QU 25, a non-dairy lactic acid bacterium, produces optically pure L-lactic acid (>= 99.9%) via homo-fermentation when cultured in the presence of xylose at high concentrations. However, as the xylose concentration decreases, a metabolic shift to hetero-lactic fermentation occurs in this strain. Furthermore, this strain preferentially metabolizes glucose when cultured in medium containing high concentrations of both glucose and xylose, indicating that a previously uncharacterized carbon-catabolite repression system may govern the regulation of these processes. Therefore, to increase the productivity of pure L-lactate by QU 25, it is necessary to investigate this regulatory process. In this study, we performed transcriptional analyses, including RNA sequencing to analyze the transcriptome of QU 25 cultivated in the presence of various glucose and/or xylose concentrations. Our results demonstrate that there was a gradual reduction in the expression of several genes in the xylose gene cluster as the glucose concentration increased, and that there was robust transcription of the genes involved in hetero-lactic fermentation under homo-lactic fermentation conditions. The former result indicates that transcriptional regulation of genes in the xylose gene cluster is involved in the catabolite repression observed in QU 25. The latter results show that the metabolic shift between homo-and hetero-lactic fermentation in QU 25 is not caused by the transcriptional regulation of related genes under the conditions tested. We therefore propose that a yet uncharacterized transcriptional regulation process is involved in the observed catabolite repression.
机译:肠球菌MUNDTII曲25是一种非乳制品乳酸菌,当在高浓度的木糖存在下培养时,通过同种发酵产生光学纯的L-乳酸(> = 99.9%)。然而,随着木糖浓度降低,在该菌株中发生了对杂乳酸发酵的代谢移位。此外,该菌株在含有高浓度的葡萄糖和木糖的培养基中培养时优先代谢葡萄糖,表明先前无表明的碳 - 抗蛋白抑制系统可以控制这些过程的调节。因此,为了通过曲25增加纯L-乳酸的生产率,有必要研究该调节过程。在该研究中,我们进行转录分析,包括RNA测序,以分析在各种葡萄糖和/或木糖浓度存在下培养的曲25的转录组。我们的结果表明,随着葡萄糖浓度的增加,木糖基因簇中的几个基因表达逐渐减少,并且在同源乳酸发酵条件下涉及杂乳酸发酵的基因具有稳健的转录。前一种结果表明,木糖基因簇中基因的转录调节涉及在曲25中观察到的分解代谢物抑制。后一种结果表明,曲25中的同源和杂乳酸发酵之间的代谢移位不是由转录引起的在测试的条件下调节相关基因。因此,我们建议尚未表明的转录调节过程参与观察到的抗粘土抑制。

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  • 来源
    《RSC Advances 》 |2015年第113期| 共10页
  • 作者单位

    Tokyo Univ Agr Dept Biosci Setagaya Ku Tokyo 1568502 Japan;

    Tokyo Univ Agr Dept Biosci Setagaya Ku Tokyo 1568502 Japan;

    Tokyo Univ Agr Nodai Res Inst Genome Res Ctr Setagaya Ku Tokyo 1568502 Japan;

    Tokyo Univ Agr Dept Biosci Setagaya Ku Tokyo 1568502 Japan;

    Kyushu Univ Dept Biosci &

    Biotechnol Lab Microbial Technol Div Syst Bioengn Grad Sch Fac Agr Higashi Ku Fukuoka 8128581 Japan;

    Tokyo Univ Agr Dept Biosci Setagaya Ku Tokyo 1568502 Japan;

    Tokyo Univ Agr Dept Biosci Setagaya Ku Tokyo 1568502 Japan;

    Kyushu Univ Dept Biosci &

    Biotechnol Lab Microbial Technol Div Syst Bioengn Grad Sch Fac Agr Higashi Ku Fukuoka 8128581 Japan;

    Tokyo Univ Agr Dept Biosci Setagaya Ku Tokyo 1568502 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学 ;
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