Isolation of thermophilic mannanase-producing bacteria useful for mannooligosaccharide (MOS) production

Surachai Rattanasuk, Khanittha Prasertsang, Sunchai Phiwphech
{"title":"Isolation of thermophilic mannanase-producing bacteria useful for mannooligosaccharide (MOS) production","authors":"Surachai Rattanasuk, Khanittha Prasertsang, Sunchai Phiwphech","doi":"10.1109/TICST.2015.7369356","DOIUrl":null,"url":null,"abstract":"Mannanase is an enzyme that catalyzes random hydrolysis of mannosidic linkages in mannans, galactomannans, glucomannans, and galactoglucomannans. The aim of this research was to isolate the mannanolytic thermophilic bacterium useful for mannooligosaccharide (MOS) production. Thermophilic mannanase-producing bacteria were isolated from 6 soil samples collected from organic rice farm of Selaphum, Roi Et, Thailand. The bacteria were cultured using Luria-Bertani (LB) supernatant containing locust bean gum (LBG) and incubated at 60 °C for 1 hr before continued culturing at 37 °C for 47 hr. The mannanase activity was screened on LB agar containing LBG stained with iodine solution. The colonies that showed clear zone were selected. The isolates were cultured using LB supernatant containing LBG at 60 °C for 72 hr. Seven isolates exhibited the high amount of halo ratio were selected and named KS1, KS2, KS3, KS4, KS5, KS6 and KS7. Mannanase activity was also determined by DNS method using LBG (pH 7.0) as mannan source and cultured media as crude mannanase. Only KS1 and KS7 strains showed thermophilic mannanase and exhibited activities at 55-90 °C. KS1 and KS7 were identified by DNA sequencing and morphology. The results revealed that KS1 is Bacillus subtilis and KS7 is Bacillus amyloliquefaciens.","PeriodicalId":251893,"journal":{"name":"2015 International Conference on Science and Technology (TICST)","volume":"15 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2015-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2015 International Conference on Science and Technology (TICST)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/TICST.2015.7369356","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

Mannanase is an enzyme that catalyzes random hydrolysis of mannosidic linkages in mannans, galactomannans, glucomannans, and galactoglucomannans. The aim of this research was to isolate the mannanolytic thermophilic bacterium useful for mannooligosaccharide (MOS) production. Thermophilic mannanase-producing bacteria were isolated from 6 soil samples collected from organic rice farm of Selaphum, Roi Et, Thailand. The bacteria were cultured using Luria-Bertani (LB) supernatant containing locust bean gum (LBG) and incubated at 60 °C for 1 hr before continued culturing at 37 °C for 47 hr. The mannanase activity was screened on LB agar containing LBG stained with iodine solution. The colonies that showed clear zone were selected. The isolates were cultured using LB supernatant containing LBG at 60 °C for 72 hr. Seven isolates exhibited the high amount of halo ratio were selected and named KS1, KS2, KS3, KS4, KS5, KS6 and KS7. Mannanase activity was also determined by DNS method using LBG (pH 7.0) as mannan source and cultured media as crude mannanase. Only KS1 and KS7 strains showed thermophilic mannanase and exhibited activities at 55-90 °C. KS1 and KS7 were identified by DNA sequencing and morphology. The results revealed that KS1 is Bacillus subtilis and KS7 is Bacillus amyloliquefaciens.
用于甘露寡糖(MOS)生产的耐热甘露聚糖酶产菌的分离
甘露聚糖酶是一种催化甘露聚糖、半乳甘露聚糖、葡甘露聚糖和半乳葡甘露聚糖中甘露聚糖键随机水解的酶。本研究的目的是分离用于甘露寡糖(MOS)生产的甘露寡糖水解嗜热细菌。从泰国Roi Et Selaphum有机水稻农场采集的6份土壤样品中分离到嗜热甘露聚糖酶产菌。采用含有刺槐豆胶(LBG)的Luria-Bertani (LB)上清液培养,60℃孵育1小时,37℃继续培养47小时。在含LBG的LB琼脂上用碘溶液染色筛选甘露聚糖酶活性。选择有清晰区域的菌落。分离株用含LBG的LB上清液在60℃下培养72小时。选取7株光晕比较高的分离株,命名为KS1、KS2、KS3、KS4、KS5、KS6和KS7。以LBG (pH 7.0)为甘露聚糖源,培养基为粗甘露聚糖酶,采用DNS法测定甘露聚糖酶活性。只有KS1和KS7菌株表现出嗜热甘露聚糖酶,并在55 ~ 90℃时表现出活性。通过DNA测序和形态学鉴定KS1和KS7。结果表明,KS1为枯草芽孢杆菌,KS7为解淀粉芽孢杆菌。
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
自引率
0.00%
发文量
0
×
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