添加半纤维素后,红torula toruloides CBS14中甘油同化和脂质产生的增强主要与能量代谢相关基因的早期转录相关。

Giselle C Martín-Hernández, Mikołaj Chmielarz, Bettina Müller, Christian Brandt, Adrian Viehweger, Martin Hölzer, Volkmar Passoth
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引用次数: 0

摘要

背景:以前发现,当酵母在粗甘油(CG)和半纤维素水解物(CGHH)的混合物中培养时,与CG作为唯一的碳源相比,甘油形成的脂质在红圆酵母中被激活。在CG和CGHH两种培养条件下,分别收集不同培养时间点的圆环麻CBS14细胞的RNA样本,并分析在相似生理条件下培养的细胞之间的差异基因表达。结果:我们观察到与CG相比,CGHH中参与氧化磷酸化的基因和线粒体中定位的酶的转录增强。与CG相比,参与蛋白质周转的基因,包括编码核糖体蛋白、翻译延伸因子和参与构建蛋白酶体的基因,在CGHH中也显示出增强的转录。在培养10 h时,CGHH中另一组被激活的基因参与β-氧化,处理氧化应激以及木糖和芳香族化合物的降解。标准的GUT1和gut2 -甘油同化途径的潜在旁路在CGHH 10 h时也得到表达和上调。当HH的额外碳源完全消耗时,在CGHH 36 h,它们的转录减少,与CG 60 h相比,NAD+依赖性甘油-3-磷酸脱氢酶上调,产生NADH,而不是甘油分解代谢的NADPH。与在CG上生长的细胞相比,在所有生理情况下,TPI1在CGHH中上调,可能将通过甘油分解代谢形成的DHAP引导为糖酵解。编码糖酵解酶的基因在CGHH作用36 h后数量最多,此时所有额外的碳源已经消耗殆尽。结论:我们怀疑甘油同化加速和脂质生成加快的生理原因主要是提供能量的酶的激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced glycerol assimilation and lipid production in Rhodotorula toruloides CBS14 upon addition of hemicellulose primarily correlates with early transcription of energy-metabolism-related genes.

Enhanced glycerol assimilation and lipid production in Rhodotorula toruloides CBS14 upon addition of hemicellulose primarily correlates with early transcription of energy-metabolism-related genes.

Enhanced glycerol assimilation and lipid production in Rhodotorula toruloides CBS14 upon addition of hemicellulose primarily correlates with early transcription of energy-metabolism-related genes.

Enhanced glycerol assimilation and lipid production in Rhodotorula toruloides CBS14 upon addition of hemicellulose primarily correlates with early transcription of energy-metabolism-related genes.

Background: Lipid formation from glycerol was previously found to be activated in Rhodotorula toruloides when the yeast was cultivated in a mixture of crude glycerol (CG) and hemicellulose hydrolysate (CGHH) compared to CG as the only carbon source. RNA samples from R. toruloides CBS14 cell cultures grown on either CG or CGHH were collected at different timepoints of cultivation, and a differential gene expression analysis was performed between cells grown at a similar physiological situation.

Results: We observed enhanced transcription of genes involved in oxidative phosphorylation and enzymes localized in mitochondria in CGHH compared to CG. Genes involved in protein turnover, including those encoding ribosomal proteins, translation elongation factors, and genes involved in building the proteasome also showed an enhanced transcription in CGHH compared to CG. At 10 h cultivation, another group of activated genes in CGHH was involved in β-oxidation, handling oxidative stress and degradation of xylose and aromatic compounds. Potential bypasses of the standard GUT1 and GUT2-glycerol assimilation pathway were also expressed and upregulated in CGHH 10 h. When the additional carbon sources from HH were completely consumed, at CGHH 36 h, their transcription decreased and NAD+-dependent glycerol-3-phosphate dehydrogenase was upregulated compared to CG 60 h, generating NADH instead of NADPH with glycerol catabolism. TPI1 was upregulated in CGHH compared to cells grown on CG in all physiological situations, potentially channeling the DHAP formed through glycerol catabolism into glycolysis. The highest number of upregulated genes encoding glycolytic enzymes was found after 36 h in CGHH, when all additional carbon sources were already consumed.

Conclusions: We suspect that the physiological reason for the accelerated glycerol assimilation and faster lipid production, was primarily the activation of enzymes that provide energy.

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