Suppr超能文献

从……中鉴定蔗糖合酶以促进生物催化糖基化。 (你提供的原文不完整,“from”后面缺少具体内容)

Identification of sucrose synthase from to favor biocatalytic glycosylation.

作者信息

Chen Kai, Lin Lei, Ma Ruiqi, Ding Jiajie, Pan Huayi, Tao Yehui, Li Yan, Jia Honghua

机构信息

College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, China.

出版信息

Front Microbiol. 2023 Aug 15;14:1220208. doi: 10.3389/fmicb.2023.1220208. eCollection 2023.

Abstract

Sucrose synthase (SuSy, EC 2.4.1.13) is a unique glycosyltransferase (GT) for developing cost-effective glycosylation processes. Up to now, some SuSys derived from plants and bacteria have been used to recycle uridine 5'-diphosphate glucose in the reactions catalyzed by Leloir GTs. In this study, after sequence mining and experimental verification, a SuSy from (SuSy), a single-cell green alga, was overexpressed in , and its enzymatic properties were characterized. In the direction of sucrose cleavage, the specific activity of the recombinant SuSy is 9.39 U/mg at 37°C and pH 7.0, and the optimum temperature and pH were 60°C and pH 7.0, respectively. Its nucleotide preference for uridine 5'-diphosphate (UDP) was similar to plant SuSys, and the enzyme activity remained relatively high when the DMSO concentration below 25%. The mutation of the predicted -terminal phosphorylation site (S31D) significantly stimulated the activity of SuSy. When the mutant S31D of SuSy was applied by coupling the engineered glycosyltransferase UGT76G1 in a one-pot two-enzyme reaction at 10% DMSO, 50 g/L rebaudioside E was transformed into 51.06 g/L rebaudioside M in 57 h by means of batch feeding, with a yield of 76.48%. This work may reveal the lower eukaryotes as a promising resource for SuSys of industrial interest.

摘要

蔗糖合酶(SuSy,EC 2.4.1.13)是一种独特的糖基转移酶(GT),可用于开发具有成本效益的糖基化工艺。到目前为止,一些源自植物和细菌的SuSy已被用于在Leloir GTs催化的反应中循环利用尿苷5'-二磷酸葡萄糖。在本研究中,经过序列挖掘和实验验证,来自单细胞绿藻的一种SuSy( 中的SuSy)在 中过表达,并对其酶学性质进行了表征。在蔗糖裂解方向上,重组SuSy在37°C和pH 7.0时的比活性为9.39 U/mg,最适温度和pH分别为60°C和pH 7.0。其对尿苷5'-二磷酸(UDP)的核苷酸偏好与植物SuSy相似,当二甲基亚砜(DMSO)浓度低于25%时,酶活性保持相对较高。预测的 -末端磷酸化位点(S31D)的突变显著刺激了SuSy的活性。当在10% DMSO条件下,将SuSy的突变体S31D与工程化的糖基转移酶UGT76G1偶联应用于一锅双酶反应时,通过分批补料,在57小时内将50 g/L的莱鲍迪苷E转化为51.06 g/L的莱鲍迪苷M,产率为76.48%。这项工作可能揭示了低等真核生物作为具有工业应用价值的SuSy的一个有前景的资源。 (注:原文中部分括号内容缺失具体信息,翻译时保留原文格式)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18fd/10465243/a4ffec92a0b6/fmicb-14-1220208-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验