首页> 外文期刊>The Journal of biological chemistry >Diversity of Δ12 Fatty Acid Desaturases in Santalaceae and Their Role in Production of Seed Oil Acetylenic Fatty Acids
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Diversity of Δ12 Fatty Acid Desaturases in Santalaceae and Their Role in Production of Seed Oil Acetylenic Fatty Acids

机译:Santalaceae中δ12脂肪酸去饱和酶的多样性及其在种子油乙酰甘露脂肪酸生产中的作用

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Plants in the Santalaceae family, including the native cherry Exocarpos cupressiformis and sweet quandong Santalum acuminatum, accumulate ximenynic acid (trans-11-octadecen-9-ynoic acid) in their seed oil and conjugated polyacetylenic fatty acids in root tissue. Twelve full-length genes coding for microsomal Δ12 fatty acid desaturases (FADs) from the two Santalaceae species were identified by degenerate PCR. Phylogenetic analysis of the predicted amino acid sequences placed five Santalaceae FADs with Δ12 FADs, which include Arabidopsis thaliana FAD2. When expressed in yeast, the major activity of these genes was Δ12 desaturation of oleic acid, but unusual activities were also observed: i.e. Δ15 desaturation of linoleic acid as well as trans-Δ12 and trans-Δ11 desaturations of stearolic acid (9-octadecynoic acid). The trans-12-octadecen-9-ynoic acid product was also detected in quandong seed oil. The two other FAD groups (FADX and FADY) were present in both species; in a phylogenetic tree of microsomal FAD enzymes, FADX and FADY formed a unique clade, suggesting that are highly divergent. The FADX group enzymes had no detectable Δ12 FAD activity but instead catalyzed cis-Δ13 desaturation of stearolic acid when expressed in yeast. No products were detected for the FADY group when expressed recombinantly. Quantitative PCR analysis showed that the FADY genes were expressed in leaf rather than developing seed of the native cherry. FADs with promiscuous and unique activities have been identified in Santalaceae and explain the origin of some of the unusual lipids found in this plant family.
机译:Santalaceae家族中的植物,包括天然樱桃Exocarpos Cupressiformis和Sweet Quandong Santalum Acuminatum,在其种子油和缀合的聚乙炔脂肪酸中累积Ximenynic acid(反式-11-十八碳酸-9-酮酸)在根组织中。通过简化PCR鉴定了来自两种Santalaceae物种的微粒Δ12脂肪酸去饱和酶(FADS)的12个全长基因。预测氨基酸序列的系统发育分析置于δ12时的五种仙人掌,其中包括拟南芥FAD2。当在酵母中表达时,这些基因的主要活性为δ12的油酸去饱和,但也观察到不寻常的活性:即延长酸的δ15除去δ12和硬olid酸的反式Δ12和反式Δ11去饱和(9-十八炔内酸)。在滨东籽油中还检测到反式-12-十八加入-9-奈瑟酸产物。两种物种都存在另外两个的FAD组(Fadx和Fady);在微粒体FAD酶的系统发育树中,FADX和FADY形成了独特的思工,表明这是高度发散的。 FADX基团酶没有可检测的Δ12时活性,而是当在酵母中表达时催化硬糖酸的CIS-Δ13去饱和。在重组表达时,对于Fady组没有检测到产物。定量PCR分析表明,FADY基因在叶中表达而不是天然樱桃的种子。 Santalaceae鉴定出杂乱和独特的活动的推出,并解释了该植物家族中发现的一些异常脂质的起源。

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