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酿酒酵母中,II号和VII号染色体上的DNA序列编码丙酮酸羧化酶同工酶:丙酮酸羧化酶缺陷型菌株的分析

DNA sequences in chromosomes II and VII code for pyruvate carboxylase isoenzymes in Saccharomyces cerevisiae: analysis of pyruvate carboxylase-deficient strains.

作者信息

Stucka R, Dequin S, Salmon J M, Gancedo C

机构信息

Institut für Physiologische Chemie, Biochemie und Zellbiologie, Universität, München, Federal Republic of Germany.

出版信息

Mol Gen Genet. 1991 Oct;229(2):307-15. doi: 10.1007/BF00272171.

Abstract

A gene encoding pyruvate carboxylase has previously been isolated from Saccharomyces cerevisiae. We have isolated a second gene, PYC2, from the same organism also encoding a pyruvate carboxylase. The gene PYC2 is situated on the right arm of chromosome II between the DUR 1, 2 markers and the telomere. We localized the previously isolated gene, which we designate PYC1, to chromosome VII. Disruption of either of the genes did not produce marked changes in the phenotype. However, simultaneous disruption of both genes resulted in inability to grow on glucose as sole carbon source, unless aspartate was added to the medium. This indicates that in wild-type yeast there is no bypass for the reaction catalysed by pyruvate carboxylase. The coding regions of both genes exhibit a homology of 90% at the amino acid level and 85% at the nucleotide level. No appreciable homology was found in the corresponding flanking regions. No differences in the Km values for ATP or pyruvate were observed between the enzymes obtained from strains carrying inactive, disrupted versions of one or other of the genes.

摘要

先前已从酿酒酵母中分离出一个编码丙酮酸羧化酶的基因。我们又从同一生物体中分离出了另一个基因PYC2,它也编码丙酮酸羧化酶。基因PYC2位于第二条染色体右臂上,介于DUR 1、2标记和端粒之间。我们将先前分离出的基因(命名为PYC1)定位到了第七条染色体上。任一基因的破坏都未在表型上产生明显变化。然而,两个基因同时被破坏会导致无法在以葡萄糖作为唯一碳源的培养基上生长,除非向培养基中添加天冬氨酸。这表明在野生型酵母中,不存在丙酮酸羧化酶所催化反应的旁路。两个基因的编码区在氨基酸水平上具有90%的同源性,在核苷酸水平上具有85%的同源性。在相应的侧翼区域未发现明显的同源性。在携带一个或另一个基因的无活性、被破坏版本的菌株所获得的酶之间,未观察到ATP或丙酮酸的Km值有差异。

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