Kanayama N, Ueda M, Atomi H, Tanaka A
Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Japan.
J Bacteriol. 1998 Feb;180(3):690-8. doi: 10.1128/JB.180.3.690-698.1998.
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.
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。