δ-(L-α-Aminoadipyl)-L-cysteinyl-D-valine synthetase, that mediates the first committed step in penicillin biosynthesis, is a cytosolic enzyme

被引:40
作者
van der Lende, TR
de Kamp, M
van den Berg, M
Sjollema, K
Bovenberg, RAL
Veenhuis, M
Konings, WN
Driessen, AJM
机构
[1] Univ Groningen, Groningen Biomol Sci & Biotechnol Inst, Dept Mol Microbiol, NL-9750 AA Haren, Netherlands
[2] DSM Anti Infect, NL-2600 AK Delft, Netherlands
[3] Univ Groningen, Dept Eukraryotic Microbiol & Electron Microscopy, Groningen Biomol Sci & Biotechnol Inst, NL-9750 AA Haren, Netherlands
关键词
beta-lactam antibiotics; compartmentalization; penicillin biosynthesis; peptide synthetase; secondary metabolism; vacuole;
D O I
10.1016/S1087-1845(02)00036-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Penicillin biosynthesis by Penicillium chrysogenum is a compartmentalized process. The first catalytic step is mediated by delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine synthetase (ACV synthetase), a high molecular mass enzyme that condenses the amino acids L-alpha-aminoadipate, L-cysteme, and L-valine into the tripeptide ACV. ACV synthetase has previously been localized to the vacuole where it is thought to utilize amino acids from the vacuolar pools. We localized ACV synthetase by subcellular fractionation and immunoelectron microscopy under conditions that prevented proteolysis and found it to co-localize with isopenicillin N synthetase in the cytosol, while acyltransferase localizes in microbodies. These data imply that the key enzymatic steps in penicillin biosynthesis are confined to only two compartments, i.e., the cytosol and microbody. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:49 / 55
页数:7
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