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一项对显示酿酒酵母Pet-表型的cls11突变体的多核磁共振研究。

A multinuclear magnetic resonance study of a cls11 mutant showing the Pet- phenotype of Saccharomyces cerevisiae.

作者信息

Galons J P, Tanida I, Ohya Y, Anraku Y, Arata Y

机构信息

Department of Physical Chemistry, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.

出版信息

Eur J Biochem. 1990 Oct 5;193(1):111-9. doi: 10.1111/j.1432-1033.1990.tb19311.x.

Abstract

Energetic and intermediary metabolism was studied in a Pet- mutant of Saccharomyces cerevisiae with a calcium-sensitive phenotype that shows an inability to grow when cultured in a medium containing non-fermentable substrates. The perchloric acid extracts were prepared from suspensions of cls11 mutant and wild-type cells incubated with [1,3-13C]glycerol or [2-13]acetate, and analyzed by 31P, 13C and 1H NMR. 31P- and 1H-NMR spectra showed significant differences between cls11 and wild-type cells at the level of amino acids, the storage carbohydrate trehalose (higher in mutant cells), and sugar phosphates (higher in wild-type cells). 13C-NMR spectra revealed major differences in the steady-state labelling of glutamate carbons. For incubations with [1,3-13C]glycerol, we estimated from the relative 13C enrichment of glutamate carbons that acetyl-CoA C2 is 43% C13 labelled in wild-type and 10% 13C labelled in mutant cells, respectively. For incubations with [2-13C]acetate, we calculated that the ratio of the relative flux through the glyoxylate shunt versus oxidative reactions is 58% in wild-type cells and 44% in the cls11 mutant cells. Again, a dilution of the relative enrichment of C2 of acetyl-CoA was observed in the mutant cells (89%) compared to the wild-type cells (97%). These results are discussed in terms of pleiotropic defects in non-fermentable carbon metabolism in mutant cells.

摘要

在酿酒酵母的一个Pet-突变体中研究了能量代谢和中间代谢,该突变体具有钙敏感表型,当在含有非发酵性底物的培养基中培养时表现出生长无能。从与[1,3-¹³C]甘油或[2-¹³C]乙酸孵育的cls11突变体细胞和野生型细胞的悬浮液中制备高氯酸提取物,并通过³¹P、¹³C和¹H NMR进行分析。³¹P-NMR和¹H-NMR光谱显示,cls11细胞和野生型细胞在氨基酸、储存碳水化合物海藻糖(突变体细胞中含量较高)和糖磷酸酯(野生型细胞中含量较高)水平上存在显著差异。¹³C-NMR光谱揭示了谷氨酸碳稳态标记的主要差异。对于用[1,3-¹³C]甘油进行的孵育,我们从谷氨酸碳的相对¹³C富集估计,野生型细胞中乙酰辅酶A C2的¹³C标记率为43%,突变体细胞中为10%。对于用[2-¹³C]乙酸进行的孵育,我们计算出野生型细胞中通过乙醛酸循环与氧化反应的相对通量比为58%,cls11突变体细胞中为44%。同样,与野生型细胞(97%)相比,突变体细胞中乙酰辅酶A C2的相对富集出现了稀释(89%)。根据突变体细胞中非发酵性碳代谢的多效性缺陷对这些结果进行了讨论。

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