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本文引用的文献

1
Investigating xylose metabolism in recombinant Saccharomyces cerevisiae via 13C metabolic flux analysis.通过 13C 代谢通量分析研究重组酿酒酵母中的木糖代谢。
Microb Cell Fact. 2013 Nov 18;12:114. doi: 10.1186/1475-2859-12-114.
2
Fermentation of xylose causes inefficient metabolic state due to carbon/energy starvation and reduced glycolytic flux in recombinant industrial Saccharomyces cerevisiae.木糖发酵会导致重组工业酿酒酵母因碳/能饥饿和降低的糖酵解通量而进入低效代谢状态。
PLoS One. 2013 Jul 9;8(7):e69005. doi: 10.1371/journal.pone.0069005. Print 2013.
3
Kinetic isotope effects significantly influence intracellular metabolite (13) C labeling patterns and flux determination.动力学同位素效应对细胞内代谢物 (13)C 标记模式和通量测定有显著影响。
Biotechnol J. 2013 Sep;8(9):1080-9. doi: 10.1002/biot.201200276. Epub 2013 Aug 5.
4
Xylose isomerase overexpression along with engineering of the pentose phosphate pathway and evolutionary engineering enable rapid xylose utilization and ethanol production by Saccharomyces cerevisiae.木糖异构酶过表达以及戊糖磷酸途径工程和进化工程使酿酒酵母能够快速利用木糖并生产乙醇。
Metab Eng. 2012 Nov;14(6):611-22. doi: 10.1016/j.ymben.2012.07.011. Epub 2012 Aug 16.
5
Dynamic metabolomics differentiates between carbon and energy starvation in recombinant Saccharomyces cerevisiae fermenting xylose.动态代谢组学可区分重组酿酒酵母发酵木糖过程中的碳饥饿和能量饥饿。
Biotechnol Biofuels. 2012 May 15;5(1):34. doi: 10.1186/1754-6834-5-34.
6
High expression of XYL2 coding for xylitol dehydrogenase is necessary for efficient xylose fermentation by engineered Saccharomyces cerevisiae.高表达编码木酮糖脱氢酶的 XYl2 对于工程化酿酒酵母高效发酵木糖是必需的。
Metab Eng. 2012 Jul;14(4):336-43. doi: 10.1016/j.ymben.2012.04.001. Epub 2012 Apr 13.
7
Evolutionary engineering of Saccharomyces cerevisiae for efficient aerobic xylose consumption.酿酒酵母有氧木糖消耗的进化工程。
FEMS Yeast Res. 2012 Aug;12(5):582-97. doi: 10.1111/j.1567-1364.2012.00808.x. Epub 2012 Apr 30.
8
A molecular transporter engineering approach to improving xylose catabolism in Saccharomyces cerevisiae.采用分子转运器工程方法提高酿酒酵母木糖代谢。
Metab Eng. 2012 Jul;14(4):401-11. doi: 10.1016/j.ymben.2012.03.004. Epub 2012 Mar 18.
9
Mapping photoautotrophic metabolism with isotopically nonstationary (13)C flux analysis.运用同位素非稳态(13)C 通量分析进行光自养代谢作图。
Metab Eng. 2011 Nov;13(6):656-65. doi: 10.1016/j.ymben.2011.08.002. Epub 2011 Sep 1.
10
Engineered Saccharomyces cerevisiae capable of simultaneous cellobiose and xylose fermentation.能够同时发酵纤维二糖和木糖的工程酿酒酵母。
Proc Natl Acad Sci U S A. 2011 Jan 11;108(2):504-9. doi: 10.1073/pnas.1010456108. Epub 2010 Dec 27.

表达木糖异构酶的木糖消耗型酿酒酵母菌株的代谢组学和(13)C代谢通量分析。

Metabolomic and (13)C-metabolic flux analysis of a xylose-consuming Saccharomyces cerevisiae strain expressing xylose isomerase.

作者信息

Wasylenko Thomas M, Stephanopoulos Gregory

机构信息

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, 02139, Massachussetts.

出版信息

Biotechnol Bioeng. 2015 Mar;112(3):470-83. doi: 10.1002/bit.25447. Epub 2014 Nov 24.

DOI:10.1002/bit.25447
PMID:25311863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4801006/
Abstract

Over the past two decades, significant progress has been made in the engineering of xylose-consuming Saccharomyces cerevisiae strains for production of lignocellulosic biofuels. However, the ethanol productivities achieved on xylose are still significantly lower than those observed on glucose for reasons that are not well understood. We have undertaken an analysis of central carbon metabolite pool sizes and metabolic fluxes on glucose and on xylose under aerobic and anaerobic conditions in a strain capable of rapid xylose assimilation via xylose isomerase in order to investigate factors that may limit the rate of xylose fermentation. We find that during xylose utilization the flux through the non-oxidative Pentose Phosphate Pathway (PPP) is high but the flux through the oxidative PPP is low, highlighting an advantage of the strain employed in this study. Furthermore, xylose fails to elicit the full carbon catabolite repression response that is characteristic of glucose fermentation in S. cerevisiae. We present indirect evidence that the incomplete activation of the fermentation program on xylose results in a bottleneck in lower glycolysis, leading to inefficient re-oxidation of NADH produced in glycolysis.

摘要

在过去二十年中,在构建用于生产木质纤维素生物燃料的消耗木糖的酿酒酵母菌株方面取得了重大进展。然而,由于尚不清楚的原因,木糖上的乙醇生产率仍显著低于葡萄糖上的乙醇生产率。我们对一株能够通过木糖异构酶快速同化木糖的菌株在有氧和厌氧条件下葡萄糖和木糖上的中心碳代谢物池大小和代谢通量进行了分析,以研究可能限制木糖发酵速率的因素。我们发现,在木糖利用过程中,通过非氧化戊糖磷酸途径(PPP)的通量很高,但通过氧化PPP的通量很低,这突出了本研究中所用菌株的一个优势。此外,木糖未能引发酿酒酵母中葡萄糖发酵特有的完全碳分解代谢物阻遏反应。我们提供间接证据表明,木糖发酵程序的不完全激活导致了低聚糖酵解的瓶颈,从而导致糖酵解中产生的NADH再氧化效率低下。