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酿酒酵母对高二氧化碳浓度的生理和全基因组转录反应。

Physiological and genome-wide transcriptional responses of Saccharomyces cerevisiae to high carbon dioxide concentrations.

作者信息

Aguilera Jaime, Petit Thomas, de Winde Johannes H, Pronk Jack T

机构信息

Department of Biotechnology, Delft University of Technology, Julianalaan 67, 2628 BC Delft, The Netherlands.

出版信息

FEMS Yeast Res. 2005 Apr;5(6-7):579-93. doi: 10.1016/j.femsyr.2004.09.009.

Abstract

Physiological effects of carbon dioxide and impact on genome-wide transcript profiles were analysed in chemostat cultures of Saccharomyces cerevisiae. In anaerobic, glucose-limited chemostat cultures grown at atmospheric pressure, cultivation under CO(2)-saturated conditions had only a marginal (<10%) impact on the biomass yield. Conversely, a 25% decrease of the biomass yield was found in aerobic, glucose-limited chemostat cultures aerated with a mixture of 79% CO(2) and 21% O(2). This observation indicated that respiratory metabolism is more sensitive to CO(2) than fermentative metabolism. Consistent with the more pronounced physiological effects of CO(2) in respiratory cultures, the number of CO(2)-responsive transcripts was higher in aerobic cultures than in anaerobic cultures. Many genes involved in mitochondrial functions showed a transcriptional response to elevated CO(2) concentrations. This is consistent with an uncoupling effect of CO(2) and/or intracellular bicarbonate on the mitochondrial inner membrane. Other transcripts that showed a significant transcriptional response to elevated CO(2) included NCE103 (probably encoding carbonic anhydrase), PCK1 (encoding PEP carboxykinase) and members of the IMD gene family (encoding isozymes of inosine monophosphate dehydrogenase).

摘要

在酿酒酵母的恒化器培养物中分析了二氧化碳的生理效应及其对全基因组转录谱的影响。在大气压下生长的厌氧、葡萄糖限制的恒化器培养物中,在二氧化碳饱和条件下培养对生物量产量的影响微乎其微(<10%)。相反,在用79%二氧化碳和21%氧气的混合物通气的需氧、葡萄糖限制的恒化器培养物中,生物量产量下降了25%。这一观察结果表明,呼吸代谢比发酵代谢对二氧化碳更敏感。与二氧化碳在呼吸培养物中更明显的生理效应一致,需氧培养物中二氧化碳响应转录本的数量高于厌氧培养物。许多参与线粒体功能的基因对升高的二氧化碳浓度表现出转录反应。这与二氧化碳和/或细胞内碳酸氢盐对线粒体内膜的解偶联作用一致。对升高的二氧化碳表现出显著转录反应的其他转录本包括NCE103(可能编码碳酸酐酶)、PCK1(编码磷酸烯醇式丙酮酸羧激酶)和IMD基因家族成员(编码肌苷单磷酸脱氢酶同工酶)。

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