Highly specific methyl-end fatty-acid desaturases of trypanosomatids

被引:19
作者
Alloatti, Andres [1 ]
Uttaro, Antonio D. [1 ]
机构
[1] Univ Nacl Rosario, Fac Ciencias Bioquim & Farmaceut, Dept Microbiol, CONICET,Inst Biol Mol & Celular Rosario IBR, RA-2000 Rosario, Santa Fe, Argentina
关键词
Trypanosoma; Leishmania; Unsaturated fatty acids; Methyl-end desaturases; Regioselectivity; SACCHAROMYCES-CEREVISIAE; OLEATE DESATURASE; ENDOPLASMIC-RETICULUM; SEQUENCE ALIGNMENT; MEMBRANE-PROTEINS; EXPRESSION; LIPIDS; BIOSYNTHESIS; BRUCEI; ENZYME;
D O I
10.1016/j.molbiopara.2010.10.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A detailed analysis of the trypanosomatids' genome projects revealed the presence of genes predicted to encode fatty-acid desaturases of the methyl-end type (MED). After cloning and functional characterization of all identified genes, it can be concluded that Trypanosome cruzi contains two MEDs with oleate desaturase (OD) activities whereas Leishmania major contains one OD and two active linoleate desaturases (LD). All characterized ODs are highly specific for oleate (18:1 Delta 9) as substrate, presenting a v + 3 regioselectivity, although palmitoleate (16:1 Delta 9) can be desaturated as well, but to a lesser extent. L major LD appears to use exclusively linoleate (18:2n-6), converting it into alpha-linolenate (18:3n-3). This strong specificity assures no further conversion of polyunsaturated fatty acids (PUFAs) of the n-6 series into the n-3 series, downstream in the PUFA biosynthesis pathway. This characterization completes the identification of all enzymes involved in PUFA biosynthesis in a parasitic protist. Differently from their Trypanosome brucei orthologue, T. cruzi and L major ODs were more active when expressed either, in the presence of trienoic fatty acids or at higher temperatures. This could be evidence for a differential post-translational regulation of these enzymes as a result of direct sensing of environmentally dependent parameters such as membrane fluidity. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:126 / 132
页数:7
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