首页> 美国卫生研究院文献>other >Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans
【2h】

Agdc1p – a Gallic Acid Decarboxylase Involved in the Degradation of Tannic Acid in the Yeast Blastobotrys (Arxula) adeninivorans

机译:Agdc1p –没食子酸脱羧酶参与降解酵母破壁植物(Arxula)腺嘌呤中的单宁酸

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Tannins and hydroxylated aromatic acids, such as gallic acid (3,4,5-trihydroxybenzoic acid), are plant secondary metabolites which protect plants against herbivores and plant-associated microorganisms. Some microbes, such as the yeast Arxula adeninivorans are resistant to these antimicrobial substances and are able to use tannins and gallic acid as carbon sources. In this study, the Arxula gallic acid decarboxylase (Agdc1p) which degrades gallic acid to pyrogallol was characterized and its function in tannin catabolism analyzed. The enzyme has a higher affinity for gallic acid (Km −0.7 ± 0.2 mM, kcat −42.0 ± 8.2 s−1) than to protocatechuic acid (3,4-dihydroxybenzoic acid) (Km −3.2 ± 0.2 mM, kcat −44.0 ± 3.2 s−1). Other hydroxylated aromatic acids, such as 3-hydroxybenzoic acid, 4-hydroxybenzoic acid, 2,3-dihydroxybenzoic acid, 2,4-dihydroxybenzoic acid and 2,5-dihydroxybenzoic acid are not gallic acid decarboxylase substrates. A. adeninivorans G1212/YRC102-AYNI1-AGDC1, which expresses the AGDC1 gene under the control of the strong nitrate inducible AYNI1 promoter achieved a maximum gallic acid decarboxylase activity of 1064.4 U/l and 97.5 U/g of dry cell weight in yeast grown in minimal medium with nitrate as nitrogen source and glucose as carbon source. In the same medium, gallic acid decarboxylase activity was not detected for the control strain G1212/YRC102 with AGDC1 expression under the control of the endogenous promoter. Gene expression analysis showed that AGDC1 is induced by gallic acid and protocatechuic acid. In contrast to G1212/YRC102-AYNI1-AGDC1 and G1212/YRC102, A. adeninivorans G1234 [Δagdc1] is not able to grow on medium with gallic acid as carbon source but can grow in presence of protocatechuic acid. This confirms that Agdc1p plays an essential role in the tannic acid catabolism and could be useful in the production of catechol and cis,cis-muconic acid. However, the protocatechuic acid catabolism via Agdc1p to catechol seems to be not the only degradation pathway.
机译:单宁和羟基化的芳香酸,如没食子酸(3,4,5-三羟基苯甲酸),是植物的次生代谢产物,可保护植物免受草食动物和与植物相关的微生物的侵害。某些微生物(例如酵母Arxula adeninivorans)对这些抗菌物质具有抵抗力,并且能够使用单宁和没食子酸作为碳源。在这项研究中,表征了将没食子酸降解为邻苯三酚的Arxula没食子酸脱羧酶(Agdc1p),并分析了其在单宁分解代谢中的功能。该酶对没食子酸(Km -0.7±0.2 mM,kcat -42.0±8.2 s -1 )的亲和力高于对原儿茶酸(3,4-二羟基苯甲酸)(Km -3.2± 0.2 mM,kcat -44.0±3.2 s -1 )。其他羟基化芳族酸,例如3-羟基苯甲酸,4-羟基苯甲酸,2,3-二羟基苯甲酸,2,4-二羟基苯甲酸和2,5-二羟基苯甲酸不是没食子酸脱羧酶底物。在强硝酸盐诱导型AYNI1启动子的控制下表达AGDC1基因的A. adeninivorans G1212 / YRC102-AYNI1-AGDC1在酵母生长过程中实现了最大没食子酸脱羧酶活性1064.4 U / l和97.5 U / g干细胞重在以硝酸盐为氮源,葡萄糖为碳源的基本培养基中。在同一培养基中,未检测到内源启动子控制下具有AGDC1表达的对照菌株G1212 / YRC102的没食子酸脱羧酶活性。基因表达分析表明,没食子酸和原儿茶酸诱导AGDC1。与G1212 / YRC102-AYNI1-AGDC1和G1212 / YRC102相比,A。adeninivorans G1234 [Δagdc1]不能在以没食子酸为碳源的培养基上生长,但可以在原儿茶酸存在下生长。这证实了Agdc1p在单宁酸分解代谢中起着至关重要的作用,可用于生产儿茶酚和顺式,顺式-粘康酸。然而,通过Agdc1p分解为儿茶酚的原儿茶酸似乎不是唯一的降解途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号