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从海洋芽孢杆菌中鉴定一种新壳聚糖酶及其水解产物的抗氧化活性。

Characterization of a New Chitosanase from a Marine Bacillus sp. and the Anti-Oxidant Activity of Its Hydrolysate.

机构信息

College of Basic Medicine, Qingdao University, Qingdao 266071, China.

出版信息

Mar Drugs. 2020 Feb 19;18(2):126. doi: 10.3390/md18020126.

DOI:10.3390/md18020126
PMID:32092959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7073567/
Abstract

Chitooligosaccharide (COS) has been recognized to exhibit efficient anti-oxidant activity. Enzymatic hydrolysis using chitosanases can retain all the amino and hydroxyl groups of chitosan, which are necessary for its activity. In this study, a new chitosanase encoding gene, , was cloned from the marine sp. Q1098 and expressed in . The recombinant chitosanase, CsnQ, showed maximal activity at pH 5.31 and 60 °C. Determination of CsnQ pH-stability showed that CsnQ could retain more than 50% of its activity over a wide pH, from 3.60 to 9.80. CsnQ is an endo-type chitosanase, yielding chitodisaccharide as the main product. Additionally, in vitro and in vivo analyses indicated that chitodisaccharide possesses much more effective anti-oxidant activity than glucosamine and low molecular weight chitosan (LMW-CS) (~5 kDa). Notably, to our knowledge, this is the first evidence that chitodisaccharide is the minimal COS fragment required for free radical scavenging.

摘要

壳寡糖(COS)已被证实具有高效的抗氧化活性。壳聚糖酶的酶解可以保留壳聚糖所有的氨基和羟基,这些基团是其活性所必需的。在这项研究中,从海洋 sp. Q1098 中克隆了一种新的壳聚糖酶编码基因 ,并在 中表达。重组壳聚糖酶 CsnQ 在 pH5.31 和 60°C 时表现出最大活性。CsnQ 的 pH 稳定性测定表明,CsnQ 在 pH3.60 到 9.80 的较宽范围内可以保留超过 50%的活性。CsnQ 是一种内切型壳聚糖酶,主要产物为壳二糖。此外,体外和体内分析表明,壳二糖的抗氧化活性比氨基葡萄糖和低分子量壳聚糖(LMW-CS)(~5 kDa)强得多。值得注意的是,据我们所知,这是壳二糖是用于清除自由基的最小 COS 片段的第一个证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/dedc96fa0907/marinedrugs-18-00126-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/c7a7af80717a/marinedrugs-18-00126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/0a558f912b44/marinedrugs-18-00126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/9b9785662cc1/marinedrugs-18-00126-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/06fe30eeca3a/marinedrugs-18-00126-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/dedc96fa0907/marinedrugs-18-00126-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/c7a7af80717a/marinedrugs-18-00126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/0a558f912b44/marinedrugs-18-00126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/9b9785662cc1/marinedrugs-18-00126-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/06fe30eeca3a/marinedrugs-18-00126-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af6d/7073567/dedc96fa0907/marinedrugs-18-00126-g005.jpg

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