Wiberg E, Edwards P, Byrne J, Stymne S, Dehesh K
Calgene, Davis, CA 95616, USA.
Planta. 2000 Dec;212(1):33-40. doi: 10.1007/s004250000361.
The composition and positional distribution of lipids in developing and mature transgenic Brassica napus seeds accumulating up to 7 mol% of caprylate (8:0), 29 mol% caprate (10:0) or 63 mol% of laurate (12:0) were examined. The accumulation of 8:0 and 10:0 resulted from over-expression of the medium-chain-specific thioesterase (Ch FatB2) alone or together with the respective chain-length-specific condensing enzyme (Ch KASIV). Seeds containing high levels of 12:0 were obtained from plants expressing bay thioesterase (BTE) alone or crossed with a line over-expressing the coconut lysophosphatidic acid acyltransferase (LPAAT), an enzyme responsible for the increase in acylation of 12:0 at the sn-2 position. In all instances, 10:0 and 12:0 fatty acids were present in substantial amounts in phosphatidylcholine during seed development with a drastic decrease of 80-90% in mature seeds. At all stages of seed development however, 8:0 was barely detectable in this membrane lipid. Altogether, these results indicate that these transgenic seeds exclude and/or remove the medium-chain fatty acids from their membrane and that this mechanism(s) is more effective with the shorter-chain fatty acids. Furthermore, seeds of 8:0- and 10:0-producing lines had only negligible levels of these fatty acids present in the sn-2 position of the triacylglycerols. In contrast, all 12:0-producing seeds had a substantial amount of this fatty acid in the sn-2 position of the triacylglycerols, suggesting that the endogenous LPAAT is able to acylate 12:0 if no other acyl-CoA species are available.
对发育中和成熟的转基因甘蓝型油菜种子中的脂质组成和位置分布进行了研究,这些种子积累了高达7摩尔%的辛酸(8:0)、29摩尔%的癸酸(10:0)或63摩尔%的月桂酸(12:0)。8:0和10:0的积累是由于中链特异性硫酯酶(Ch FatB2)单独过表达或与各自链长特异性缩合酶(Ch KASIV)共同过表达所致。含有高水平12:0的种子是从单独表达海湾硫酯酶(BTE)或与过表达椰子溶血磷脂酸酰基转移酶(LPAAT)的品系杂交的植株中获得的,LPAAT是一种负责sn-2位12:0酰化增加的酶。在所有情况下,种子发育过程中磷脂酰胆碱中大量存在10:0和12:0脂肪酸,成熟种子中急剧减少80 - 90%。然而,在种子发育的所有阶段,这种膜脂中几乎检测不到8:0。总之,这些结果表明,这些转基因种子将中链脂肪酸排除和/或从其膜中去除,并且这种机制对较短链脂肪酸更有效。此外,产生8:0和10:0的品系的种子在三酰甘油的sn-2位中这些脂肪酸的含量极低。相比之下,所有产生12:0的种子在三酰甘油的sn-2位中都有大量这种脂肪酸,这表明如果没有其他酰基辅酶A种类,内源性LPAAT能够将12:0酰化。