...
首页> 外文期刊>Applied and Environmental Microbiology >Cloning and Characterization of the xyl1 Gene, Encoding an NADH-Preferring Xylose Reductase from Candida parapsilosis, and Its Functional Expression in Candida tropicalis
【24h】

Cloning and Characterization of the xyl1 Gene, Encoding an NADH-Preferring Xylose Reductase from Candida parapsilosis, and Its Functional Expression in Candida tropicalis

机译:xyl1基因的克隆和表征,编码NADH偏爱假丝酵母的木糖还原酶,及其在热带念珠菌中的功能性表达

获取原文
           

摘要

Xylose reductase (XR) is a key enzyme in d-xylose metabolism, catalyzing the reduction of d-xylose to xylitol. An NADH-preferring XR was purified to homogeneity from Candida parapsilosis KFCC-10875, and the xyl1 gene encoding a 324-amino-acid polypeptide with a molecular mass of 36,629 Da was subsequently isolated using internal amino acid sequences and 5′ and 3′ rapid amplification of cDNA ends. The C. parapsilosis XR showed high catalytic efficiency (kcat/Km = 1.46 s?1 mM?1) for d-xylose and showed unusual coenzyme specificity, with greater catalytic efficiency with NADH (kcat/Km = 1.39 × 104 s?1 mM?1) than with NADPH (kcat/Km = 1.27 × 102 s?1 mM?1), unlike all other aldose reductases characterized. Studies of initial velocity and product inhibition suggest that the reaction proceeds via a sequentially ordered Bi Bi mechanism, which is typical of XRs. Candida tropicalis KFCC-10960 has been reported to have the highest xylitol production yield and rate. It has been suggested, however, that NADPH-dependent XRs, including the XR of C. tropicalis, are limited by the coenzyme availability and thus limit the production of xylitol. The C. parapsilosis xyl1 gene was placed under the control of an alcohol dehydrogenase promoter and integrated into the genome of C. tropicalis. The resulting recombinant yeast, C. tropicalis BN-1, showed higher yield and productivity (by 5 and 25%, respectively) than the wild strain and lower production of by-products, thus facilitating the purification process. The XRs partially purified from C. tropicalis BN-1 exhibited dual coenzyme specificity for both NADH and NADPH, indicating the functional expression of the C. parapsilosis xyl1 gene in C. tropicalis BN-1. This is the first report of the cloning of an xyl1 gene encoding an NADH-preferring XR and its functional expression in C. tropicalis, a yeast currently used for industrial production of xylitol.
机译:木糖还原酶(XR)是D-木糖代谢中的关键酶,催化D-木糖还原为木糖醇。从副念珠菌KFCC-10875中纯化出首选NADH的XR,使其具有同质性,随后使用内部氨基酸序列,5'和3'快速分离编码分子量为36629 Da的324个氨基酸的多肽的xyl1基因cDNA末端的扩增。 C. parapsilosis XR对D-木糖显示出高催化效率(kcat / Km = 1.46 s?1 mM?1),并显示出不同寻常的辅酶特异性,而NADH的催化效率更高(kcat / Km = 1.39×104 s?1 mM)。与使用NADPH(kcat / Km = 1.27×102 s?1 mM?1)相比,α1)不同于所有其他醛糖还原酶。初始速度和产物抑制的研究表明,反应是通过顺序排列的Bi Bi机理进行的,这是XR的典型特征。据报道,热带假丝酵母KFCC-10960的木糖醇产量和产率最高。然而,已经提出,依赖NADPH的XR,包括热带假丝酵母的XR,受到辅酶可用性的限制,因此限制了木糖醇的生产。副疟原虫xyl1基因被置于乙醇脱氢酶启动子的控制下,并整合到热带假单胞菌的基因组中。所得重组酵母C.tropicis BN-1与野生菌株相比显示出更高的产量和生产率(分别提高了5%和25%),副产物的产生也降低了,从而促进了纯化过程。从热带念珠菌BN-1中部分纯化的XR对NADH和NADPH均显示双重辅酶特异性,表明副热带念珠菌xyl1基因在热带念珠菌BN-1中具有功能性表达。这是克隆编码NADH优先XR的xyl1基因及其在热带假丝酵母中的功能性表达的第一个报道,热带假丝酵母目前用于工业生产木糖醇。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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