Xylooligosaccharides from Pretreated Rice Bran Produced by Immobilized Xylanase

IF 3.1 3区 工程技术 Q3 ENERGY & FUELS
Letícia Persilva Fernandes, Rafaela Zandonade Ventorim, Micael Garcia de Oliveira, Lucas Filipe Almeida, Valéria Monteze Guimarães, Gabriela Piccolo Maitan-Alfenas
{"title":"Xylooligosaccharides from Pretreated Rice Bran Produced by Immobilized Xylanase","authors":"Letícia Persilva Fernandes,&nbsp;Rafaela Zandonade Ventorim,&nbsp;Micael Garcia de Oliveira,&nbsp;Lucas Filipe Almeida,&nbsp;Valéria Monteze Guimarães,&nbsp;Gabriela Piccolo Maitan-Alfenas","doi":"10.1007/s12155-024-10770-3","DOIUrl":null,"url":null,"abstract":"<div><p>Xylooligosaccharides (XOS) are potential prebiotic ingredients for food industries, mainly obtained after xylan hydrolysis by endoxylanases. Enzyme immobilization offers opportunities for recovery and reuse, while also enhancing its physical and chemical characteristics, such as stability and catalytic efficiency. This work aimed to immobilize the SM2 xylanase derived from the <i>xynA</i> gene from <i>Orpinomyces</i> sp. PC-2 and to evaluate its potential for XOS production. For this, SM2 xylanase was immobilized using the cross-linking methodology. The free and immobilized enzymes were characterized regarding the effect of pH, temperature, and thermostability. The cross-linked enzyme aggregate was evaluated for reuse and storage conditions and used for xylooligosaccharide production. Both free and immobilized SM2 xylanase showed maximal activity at 60 °C. The immobilized enzyme was more active at acidic and neutral conditions, and the free enzyme showed greater activity at basic conditions. The half-life of the free and immobilized xylanase was 30 and 216 h, respectively. In reuse tests, enzymatic activity increased with each cycle, and there was no statistical difference in the activity of SM2 xylanase aggregate stored at 4 and 25 °C. After saccharification, xylobiose (0.895 g/L), xylotriose (0.489 g/L), and xylohexose (0.809 g/L) were detected. As a result, immobilization enhanced thermostability, shifted the pH of maximum activity to 5, facilitated reuse, and eliminated the need for refrigerated packaging. Finally, the xylooligosaccharides produced by the SM2 xylanase are known for their prebiotic role, providing potential application of the immobilized enzyme in the food industry.</p></div>","PeriodicalId":487,"journal":{"name":"BioEnergy Research","volume":"17 4","pages":"2236 - 2245"},"PeriodicalIF":3.1000,"publicationDate":"2024-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BioEnergy Research","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s12155-024-10770-3","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0

Abstract

Xylooligosaccharides (XOS) are potential prebiotic ingredients for food industries, mainly obtained after xylan hydrolysis by endoxylanases. Enzyme immobilization offers opportunities for recovery and reuse, while also enhancing its physical and chemical characteristics, such as stability and catalytic efficiency. This work aimed to immobilize the SM2 xylanase derived from the xynA gene from Orpinomyces sp. PC-2 and to evaluate its potential for XOS production. For this, SM2 xylanase was immobilized using the cross-linking methodology. The free and immobilized enzymes were characterized regarding the effect of pH, temperature, and thermostability. The cross-linked enzyme aggregate was evaluated for reuse and storage conditions and used for xylooligosaccharide production. Both free and immobilized SM2 xylanase showed maximal activity at 60 °C. The immobilized enzyme was more active at acidic and neutral conditions, and the free enzyme showed greater activity at basic conditions. The half-life of the free and immobilized xylanase was 30 and 216 h, respectively. In reuse tests, enzymatic activity increased with each cycle, and there was no statistical difference in the activity of SM2 xylanase aggregate stored at 4 and 25 °C. After saccharification, xylobiose (0.895 g/L), xylotriose (0.489 g/L), and xylohexose (0.809 g/L) were detected. As a result, immobilization enhanced thermostability, shifted the pH of maximum activity to 5, facilitated reuse, and eliminated the need for refrigerated packaging. Finally, the xylooligosaccharides produced by the SM2 xylanase are known for their prebiotic role, providing potential application of the immobilized enzyme in the food industry.

Abstract Image

Abstract Image

固定化木聚糖酶从预处理米糠中产生的木寡糖
木寡糖(XOS)是食品工业中潜在的益生元成分,主要由内源木聚糖酶水解木聚糖后获得。酶固定化为回收和再利用提供了机会,同时也提高了其物理和化学特性,如稳定性和催化效率。这项工作的目的是固定源于 PC-2 奥品霉菌 xynA 基因的 SM2 木聚糖酶,并评估其生产 XOS 的潜力。为此,采用交联法固定了 SM2 木聚糖酶。对游离酶和固定化酶的 pH 值、温度和热稳定性的影响进行了表征。对交联酶聚合体的重复使用和储存条件进行了评估,并将其用于木寡糖的生产。游离和固定的 SM2 木聚糖酶在 60 °C 时都显示出最大活性。固定化酶在酸性和中性条件下活性更高,而游离酶在碱性条件下活性更高。游离和固定化木聚糖酶的半衰期分别为 30 和 216 小时。在重复使用测试中,酶活性随着每次循环而增加,SM2 木聚糖酶聚合体在 4 ℃ 和 25 ℃ 储存时的活性没有统计学差异。糖化后可检测到木糖(0.895 克/升)、木三糖(0.489 克/升)和木六糖(0.809 克/升)。因此,固定化提高了热稳定性,将最大活性的 pH 值调至 5,方便了重复使用,并消除了冷藏包装的需要。最后,SM2 木聚糖酶产生的木寡糖具有益生作用,为固定化酶在食品工业中的应用提供了可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BioEnergy Research
BioEnergy Research ENERGY & FUELS-ENVIRONMENTAL SCIENCES
CiteScore
6.70
自引率
8.30%
发文量
174
审稿时长
3 months
期刊介绍: BioEnergy Research fills a void in the rapidly growing area of feedstock biology research related to biomass, biofuels, and bioenergy. The journal publishes a wide range of articles, including peer-reviewed scientific research, reviews, perspectives and commentary, industry news, and government policy updates. Its coverage brings together a uniquely broad combination of disciplines with a common focus on feedstock biology and science, related to biomass, biofeedstock, and bioenergy production.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信