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首页> 外文期刊>Journal of the American Oil Chemists' Society >Genetic regulation of elevated stearic acid concentration in soybean oil
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Genetic regulation of elevated stearic acid concentration in soybean oil

机译:大豆油中硬脂酸浓度升高的遗传调控

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摘要

Soybean [Glycine max (L.) Merr.] oil from commercial cultivars typically contains ca. 3% stearic acid (18:0). However, germplasm carrying different mutations at the locus governing stearic acid (Fas) may contain 3% to about 35% 18:0. Among these germplasm, a newly developed line, FAM94-41 (9% 18:0), carries a serendipitous natural mutation that is temporarily designated as the recessive fas(nc) allele, and the germplasm A6 (26% 18:0) carries the recessive fas(a) allele. Mendelian genetic analysis of progeny from FAM94-41 x A6 revealed that fas(nc) and fas(a) are allelic to each other and represent different mutations in the same structural gene. However, the gene products (enzymes) produced by these alleles are unknown. The observation that 18:0 concentrations among progeny from FAM94-41 x A6 increased primarily at the expense of unsaturated C-18 FA suggests that fas alleles may reduce either 18:0-acyl carrier protein (AcP) desaturase or 18:1-ACP thioesterase activity. However, it also is conceivable that elevated 18:0 concentrations may result from increased 3-keto-acyl-ACP synthetase (KAS) II activity. To test the latter possibility, a population was created that segregated for the fas(nc) and the fap(2) alleles (the latter of which is associated with reduced KAS-II activity). Mendelian genetic analysis showed that these alleles represent independent genes at different gene loci and interact in an additive genetic manner to increase the total saturate concentration in this population. Based on this finding, we speculate that fas alleles probably encode 18:0-ACP desaturase or 18:1-ACP thioesterase in soybeans.
机译:来自商业品种的大豆[Glycine max(L.)Merr。]油通常含有3%的硬脂酸(18:0)。但是,在控制硬脂酸(Fas)的基因座处携带不同突变的种质可能包含3%至约35%的18:0。在这些种质中,一个新开发的品系FAM94-41(9%18:0)携带一个偶然的自然突变,该突变被暂时称为隐性fas(nc)等位基因,而种质A6(26%18:0)携带隐性fas(a)等位基因。孟德尔对FAM94-41 x A6的后代进行的遗传分析表明,fas(nc)和fas(a)是相互等位的,并代表同一结构基因中的不同突变。但是,由这些等位基因产生的基因产物(酶)是未知的。 FAM94-41 x A6子代中18:0浓度的增加主要是以不饱和C-18 FA为代价的观察结果表明,fas等位基因可能会降低18:0-酰基载体蛋白(AcP)去饱和酶或18:1-ACP硫酯酶活性。然而,也可以想到的是,升高的18:0浓度可能是由于3-酮-酰基-ACP合成酶(KAS)II活性增加所致。为了测试后者的可能性,创建了一个针对fas(nc)和fap(2)等位基因(后者与降低的KAS-II活性相关)的种群。孟德尔遗传分析表明,这些等位基因代表不同基因位点的独立基因,并以累加遗传方式相互作用,以增加该种群中的总饱和浓度。基于此发现,我们推测fas等位基因可能编码大豆中的18:0-ACP去饱和酶或18:1-ACP硫酯酶。

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