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一个位于三糖利用基因座中的肠道细菌S2编码的用于降解α-查茄碱和α-茄碱的多功能酶组合。

A multifunctional enzyme portfolio for α-chaconine and α-solanine degradation in the gut bacterium S2 encoded in a trisaccharide utilization locus.

作者信息

Wang Wenqian, Du Guangzu, Yang Guangyuan, Zhang Ke, Chen Bin, Xiao Guanli

机构信息

State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, College of Plant Protection, Yunnan Agricultural University, Kunming, China.

College of Agronomy and Biotechnology, Yunnan Agricultural University, Kunming, China.

出版信息

Front Microbiol. 2022 Oct 12;13:1023698. doi: 10.3389/fmicb.2022.1023698. eCollection 2022.

Abstract

Steroidal glycoalkaloids (SGAs) are secondary metabolites commonly found in members of the family Solanaceae, including potatoes, and are toxic to pests and humans. The predominant SGAs in potato are α-chaconine and α-solanine. We previously reported that S2, a gut bacterium of the pest (potato tuber moth), can degrade α-chaconine and α-solanine in potatoes, which can improve the fitness of to feed on potatoes with a high content of toxic SGAs. S2 harbored a gene cluster containing three deglycosylase genes-, , and that were predicted encode α-rhamnosidase (RhaA), β-glucosidase (GluA), and β-galactosidase (GalA). However, there is limited information is available on the enzyme activities of the three enzymes expressed by this gene cluster and how they degrade the major toxic α-chaconine and α-solanine. In the current study, each enzyme of this gene cluster was produced by a prokaryotic expression approach and the activity of the recombinant enzymes for their target substrate and α-chaconine and α-solanine were evaluated by EPOCH microplate spectrophotometer and liquid chromatography mass spectrometry (LC-MS). The three enzymes had multifunctional activities, with RhaA and GluA could hydrolyze α-rhamnose, β-glucose, and β-galactose, while GalA can hydrolyze β-glucose and β-galactose. The degradation of α-chaconine and α-solanine was consistent with the results of the enzyme activity assays. The final product solanidine could be generated by adding RhaA or GluA alone. In conclusion, this study characterized the multifunctional activity and specific degradation pathway of these three enzymes in S2. The three multifunctional enzymes have high glycosidic hydrolysis activity and clear gene sequence information, which help facilitates understanding the detoxification mechanism of insect gut microbes. The enzymes have a broad application potential and may be valuable in the removal of toxic SGAs from for potato food consumption.

摘要

甾体糖生物碱(SGAs)是常见于茄科植物成员(包括马铃薯)中的次生代谢产物,对害虫和人类有毒。马铃薯中主要的SGAs是α-查茄碱和α-茄碱。我们之前报道过,害虫(马铃薯块茎蛾)的肠道细菌S2能够降解马铃薯中的α-查茄碱和α-茄碱,这可以提高其取食高含量有毒SGAs马铃薯的适应性。S2含有一个基因簇,其中包含三个去糖基化酶基因——rhaA、gluA和galA,预测它们编码α-鼠李糖苷酶(RhaA)、β-葡萄糖苷酶(GluA)和β-半乳糖苷酶(GalA)。然而,关于该基因簇表达的这三种酶的酶活性以及它们如何降解主要有毒的α-查茄碱和α-茄碱的信息有限。在本研究中,通过原核表达方法产生了该基因簇的每种酶,并使用Epoch微孔板分光光度计和液相色谱质谱联用仪(LC-MS)评估了重组酶对其目标底物以及α-查茄碱和α-茄碱的活性。这三种酶具有多功能活性,RhaA和GluA能够水解α-鼠李糖、β-葡萄糖和β-半乳糖,而GalA可以水解β-葡萄糖和β-半乳糖。α-查茄碱和α-茄碱的降解与酶活性测定结果一致。单独添加RhaA或GluA即可生成最终产物茄啶。总之,本研究表征了S2中这三种酶的多功能活性和特定降解途径。这三种多功能酶具有高糖苷水解活性和明确的基因序列信息,有助于理解昆虫肠道微生物的解毒机制。这些酶具有广泛的应用潜力,可能对去除马铃薯食品中的有毒SGAs有价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/274f/9597252/733d88260f96/fmicb-13-1023698-g001.jpg

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