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热带假丝酵母中硫解酶同工酶生理功能的遗传评估,该酵母可同化正构烷烃

Genetic evaluation of physiological functions of thiolase isoenzymes in the n-alkalane-assimilating yeast Candida tropicalis.

作者信息

Kanayama N, Ueda M, Atomi H, Tanaka A

机构信息

Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Japan.

出版信息

J Bacteriol. 1998 Feb;180(3):690-8. doi: 10.1128/JB.180.3.690-698.1998.

Abstract

The n-alkane-assimilating diploid yeast Candida tropicalis possesses three thiolase isozymes encoded by two pairs of alleles: cytosolic and peroxisomal acetoacetyl-coenzyme A (CoA) thiolases, encoded by CT-T1A and CT-T1B, and peroxisomal 3-ketoacyl-CoA thiolase, encoded by CT-T3A and CT-T3B. The physiological functions of these thiolases have been examined by gene disruption. The homozygous ct-t1a delta/t1bdelta null mutation abolished the activity of acetoacetyl-CoA thiolase and resulted in mevalonate auxotrophy. The homozygous ct-t3a delta/t3b delta null mutation abolished the activity of 3-ketoacyl-CoA thiolase and resulted in growth deficiency on n-alkanes (C10 to C13). All thiolase activities in this yeast disappeared with the ct-t1a delta/t1bdelta and ct-t3a delta/t3bdelta null mutations. To further clarify the function of peroxisomal acetoacetyl-CoA thiolases, the site-directed mutation leading acetoacetyl-CoA thiolase without a putative C-terminal peroxisomal targeting signal was introduced on the CT-T1A locus in the ct-t1bdelta null mutant. The truncated acetoacetyl-CoA thiolase was solely present in cytoplasm, and the absence of acetoacetyl-CoA thiolase in peroxisomes had no effect on growth on all carbon sources employed. Growth on butyrate was not affected by a lack of peroxisomal acetoacetyl-CoA thiolase, while a retardation of growth by a lack of peroxisomal 3-ketoacyl-CoA thiolase was observed. A defect of both peroxisomal isozymes completely inhibited growth on butyrate. These results demonstrated that cytosolic acetoacetyl-CoA thiolase was indispensable for the mevalonate pathway and that both peroxisomal acetoacetyl-CoA thiolase and 3-ketoacyl-CoA thiolase could participate in peroxisomal beta-oxidation. In addition to its essential contribution to the beta-oxidation of longer-chain fatty acids, 3-ketoacyl-CoA thiolase contributed greatly even to the beta-oxidation of a C4 substrate butyrate.

摘要

同化正构烷烃的二倍体酵母热带假丝酵母拥有由两对等位基因编码的三种硫解酶同工酶

胞质和过氧化物酶体乙酰乙酰辅酶A(CoA)硫解酶,分别由CT-T1A和CT-T1B编码;过氧化物酶体3-酮酰基辅酶A硫解酶,由CT-T3A和CT-T3B编码。已通过基因敲除研究了这些硫解酶的生理功能。纯合的ct-t1aΔ/t1bΔ无效突变消除了乙酰乙酰辅酶A硫解酶的活性,并导致甲羟戊酸营养缺陷。纯合的ct-t3aΔ/t3bΔ无效突变消除了3-酮酰基辅酶A硫解酶的活性,并导致在正构烷烃(C10至C13)上生长缺陷。该酵母中的所有硫解酶活性都随着ct-t1aΔ/t1bΔ和ct-t3aΔ/t3bΔ无效突变而消失。为了进一步阐明过氧化物酶体乙酰乙酰辅酶A硫解酶的功能,在ct-t1bΔ无效突变体的CT-T1A基因座上引入了导致乙酰乙酰辅酶A硫解酶没有推定的C末端过氧化物酶体靶向信号的定点突变。截短的乙酰乙酰辅酶A硫解酶仅存在于细胞质中,过氧化物酶体中缺乏乙酰乙酰辅酶A硫解酶对所使用的所有碳源上的生长没有影响。缺乏过氧化物酶体乙酰乙酰辅酶A硫解酶不影响丁酸盐上的生长,而观察到缺乏过氧化物酶体3-酮酰基辅酶A硫解酶会导致生长迟缓。两种过氧化物酶体同工酶的缺陷完全抑制了丁酸盐上的生长。这些结果表明,胞质乙酰乙酰辅酶A硫解酶对于甲羟戊酸途径是必不可少的,并且过氧化物酶体乙酰乙酰辅酶A硫解酶和3-酮酰基辅酶A硫解酶都可以参与过氧化物酶体β-氧化。除了对长链脂肪酸的β-氧化有重要贡献外,3-酮酰基辅酶A硫解酶对C4底物丁酸盐的β-氧化也有很大贡献。

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