Involvement of acyl-CoA synthetase genes in n-alkane assimilation and fatty acid utilization in yeast Yarrowia lipolytica

被引:23
|
作者
Tenagy [1 ]
Park, Jun Seok [1 ]
Iwama, Ryo [1 ]
Kobayashi, Satoshi [1 ]
Ohta, Akinori [2 ]
Horiuchi, Hiroyuki [1 ]
Fukuda, Ryouichi [1 ]
机构
[1] Univ Tokyo, Dept Biotechnol, Bunkyo Ku, Tokyo 1138657, Japan
[2] Chubu Univ, Coll Biosci & Biotechnol, Dept Biol Chem, Kasugai, Aichi 4878501, Japan
关键词
Yarrowia lipolytica; acyl-CoA synthetase; n-alkane; fatty acid; SACCHAROMYCES-CEREVISIAE HOMOLOG; BINDING-CASSETTE TRANSPORTER; DECANE ASSIMILATION; PHOSPHATIDIC-ACID; PROTEIN FAT1P; LIPID BODIES; METABOLISM; ACTIVATION; ACYLTRANSFERASE; MYRISTOYLATION;
D O I
10.1093/femsyr/fov031
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Here, we investigated the roles of YAL1 (FAA1) and FAT1 encoding acyl-CoA synthetases (ACSs) and three additional orthologs of ACS genes FAT2-FAT4 of the yeast Yarrowia lipolytica in the assimilation or utilization of n-alkanes and fatty acids. ACS deletion mutants were generated to characterize their function. The FAT1 deletion mutant exhibited decreased growth on n-alkanes of 10-18 carbons, whereas the FAA1 mutant showed growth reduction on n-alkane of 16 carbons. However, FAT2-FAT4 deletion mutants did not show any growth defects, suggesting that FAT1 and FAA1 are involved in the activation of fatty acids produced during the metabolism of n-alkanes. In contrast, deletions of FAA1 and FAT1-FAT4 conferred no defect in growth on fatty acids. The wild-type strain grew in the presence of cerulenin, an inhibitor of fatty acid synthesis, by utilizing exogenously added fatty acid or fatty acid derived from n-alkane when oleic acid or n-alkane of 18 carbons was supplemented. However, the FAA1 deletion mutant did not grow, indicating a critical role for FAA1 in the utilization of fatty acids. Fluorescent microscopic observation and biochemical analyses suggested that Fat1p is present in the peroxisome and Faa1p is localized in the cytosol and to membranes.
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页数:12
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