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多年生花生(Arachis glabrata Benth.)叶片含有羟基肉桂酰辅酶A:酒石酸羟基肉桂酰转移酶活性,并积累羟基肉桂酰酒石酸酯。

Perennial peanut (Arachis glabrata Benth.) leaves contain hydroxycinnamoyl-CoA:tartaric acid hydroxycinnamoyl transferase activity and accumulate hydroxycinnamoyl-tartaric acid esters.

作者信息

Sullivan Michael L

机构信息

US Dairy Forage Research Center, US Department of Agriculture, Agricultural Research Service, 1925 Linden Drive, Madison, WI, 53705, USA,

出版信息

Planta. 2014 May;239(5):1091-100. doi: 10.1007/s00425-014-2038-x. Epub 2014 Feb 21.

Abstract

Many plants accumulate hydroxycinnamoyl esters to protect against abiotic and biotic stresses. Caffeoyl esters in particular can be substrates for endogenous polyphenol oxidases (PPOs). Recently, we showed that perennial peanut (Arachis glabrata Benth.) leaves contain PPO and identified one PPO substrate, caftaric acid (trans-caffeoyl-tartaric acid). Additional compounds were believed to be cis- and trans-p-coumaroyl tartaric acid and cis- and trans-feruloyl-tartaric acid, but lack of standards prevented definitive identifications. Here we characterize enzymatic activities in peanut leaves to understand how caftaric acid and related hydroxycinnamoyl esters are made in this species. We show that peanut leaves contain a hydroxycinnamoyl-CoA:tartaric acid hydroxycinnamoyl transferase (HTT) activity capable of transferring p-coumaroyl, caffeoyl, and feruloyl moieties from CoA to tartaric acid (specific activities of 11 ± 2.8, 8 ± 1.8, 4 ± 0.8 pkat mg(-1) crude protein, respectively). The HTT activity was used to make cis- and trans-p-coumaroyl- and -feruloyl-tartaric acid in vitro. These products allowed definitive identification of the corresponding cis- and trans-hydroxycinnamoyl esters extracted from leaves. We tentatively identified sinapoyl-tartaric acid as another major phenolic compound in peanut leaves that likely participates in secondary reactions with PPO-generated quinones. These results suggest hydroxycinnamoyl-tartaric acid esters are made by an acyltransferase, possibly a BAHD family member, in perennial peanut. Identification of a gene encoding HTT and further characterization of the enzyme will aid in identifying determinants of donor and acceptor substrate specificity for this important class of biosynthetic enzymes. An HTT gene could also provide a means by genetic engineering for producing caffeoyl- and other hydroxycinnamoyl-tartaric acid esters in forage crops that lack them.

摘要

许多植物积累羟基肉桂酸酯以抵御非生物和生物胁迫。特别是咖啡酰酯可以作为内源性多酚氧化酶(PPO)的底物。最近,我们发现多年生花生(Arachis glabrata Benth.)叶片中含有PPO,并鉴定出一种PPO底物,咖啡酒石酸(反式咖啡酰酒石酸)。据信其他化合物为顺式和反式对香豆酰酒石酸以及顺式和反式阿魏酰酒石酸,但由于缺乏标准品而无法进行明确鉴定。在此,我们对花生叶片中的酶活性进行表征,以了解该物种中咖啡酒石酸及相关羟基肉桂酸酯是如何合成的。我们发现花生叶片含有一种羟基肉桂酰辅酶A:酒石酸羟基肉桂酰转移酶(HTT)活性,能够将对香豆酰、咖啡酰和阿魏酰基团从辅酶A转移至酒石酸(粗蛋白的比活性分别为11±2.8、8±1.8、4±0.8 pkat mg(-1))。HTT活性被用于在体外合成顺式和反式对香豆酰 - 和 - 阿魏酰酒石酸。这些产物使得从叶片中提取的相应顺式和反式羟基肉桂酸酯得以明确鉴定。我们初步鉴定芥子酰酒石酸是花生叶片中另一种主要的酚类化合物,它可能参与与PPO生成的醌的二级反应。这些结果表明羟基肉桂酰酒石酸酯是由一种酰基转移酶在多年生花生中合成的,该酰基转移酶可能是BAHD家族成员。鉴定编码HTT的基因并进一步表征该酶将有助于确定这类重要生物合成酶的供体和受体底物特异性的决定因素。一个HTT基因还可以通过基因工程手段为在缺乏这些物质的饲料作物中生产咖啡酰和其他羟基肉桂酰酒石酸酯提供一种方法。

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