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与共轭反式-δ11,顺式-δ13双键形成相关的δ12-油酸去饱和酶相关酶。

Delta 12-oleate desaturase-related enzymes associated with formation of conjugated trans-delta 11, cis-delta 13 double bonds.

作者信息

Iwabuchi Mari, Kohno-Murase Junko, Imamura Jun

机构信息

Plantech Research Institute, 1000 Kamoshida-cho, Aoba-ku, Yokohama 227-0033, Japan.

出版信息

J Biol Chem. 2003 Feb 14;278(7):4603-10. doi: 10.1074/jbc.M210748200. Epub 2002 Dec 2.

DOI:10.1074/jbc.M210748200
PMID:12464604
Abstract

Conjugated linolenic acids are present as major seed oils in several plant species. Punicic acid (or trichosanic acid) is a conjugated linolenic acid isomer containing cis-delta9, trans-delta11, cis-delta13 double bonds in the C(18) carbon chain. Here we report cDNAs, TkFac and PgFac, isolated from Trichosanthes kirilowii and Punica granatum, that encode a class of conjugases associated with the formation of trans-delta11, cis-delta13 double bonds. Expression of TkFac and PgFac in Arabidopsis seeds under transcriptional control of the seed-specific napin promoter resulted in accumulation of punicic acid up to approximately 10% (w/w) of the total seed oils. In contrast, no punicic acid was found in lipids from leaves even when the conjugases were driven under control of the cauliflower mosaic virus 35S promoter. In yeast cells grown without exogenous fatty acids in the culture medium, TkFac and PgFac expression resulted in punicic acid accumulation accompanied by 16:2delta(9cis, 12cis) and 18:2delta(9cis, 12cis) production. Thus, TkFac and PgFac are defined as bifunctional enzymes having both conjugase and delta12-oleate desaturase activity. Furthermore, we demonstrate that 16:2delta(9cis, 12cis) and 18:3delta(9cis, 12cis, 15cis) as well as 18:2delta(9cis, 12cis) are potential substrates for the conjugases to form trans-delta11 and cis-delta13 double bonds.

摘要

共轭亚麻酸在几种植物物种中作为主要种子油存在。石榴酸(或天花粉酸)是一种共轭亚麻酸异构体,在C(18)碳链中含有顺式-δ9、反式-δ11、顺式-δ13双键。在此,我们报告了从栝楼和石榴中分离出的cDNA,即TkFac和PgFac,它们编码一类与反式-δ11、顺式-δ13双键形成相关的共轭酶。在种子特异性napin启动子的转录控制下,TkFac和PgFac在拟南芥种子中的表达导致石榴酸积累,其含量高达种子总油的约10%(w/w)。相比之下,即使在花椰菜花叶病毒35S启动子的控制下驱动共轭酶,叶片脂质中也未发现石榴酸。在培养基中无外源脂肪酸生长的酵母细胞中,TkFac和PgFac的表达导致石榴酸积累,并伴有16:2δ(9顺式, 12顺式)和18:2δ(9顺式, 12顺式)的产生。因此,TkFac和PgFac被定义为具有共轭酶和δ12 -油酸去饱和酶活性的双功能酶。此外,我们证明16:2δ(9顺式, 12顺式)、18:3δ(9顺式, 12顺式, 15顺式)以及18:2δ(9顺式, 12顺式)是共轭酶形成反式-δ11和顺式-δ13双键的潜在底物。

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