Aktivitas Enzim Inulinase dan Laju Pertumbuhan Spesifik Isolat Bakteri IS-1 pada Medium Tepung Umbi Dahlia

W. Wijanarka, Maulida Aqlia, K. Kristina
{"title":"Aktivitas Enzim Inulinase dan Laju Pertumbuhan Spesifik Isolat Bakteri IS-1 pada Medium Tepung Umbi Dahlia","authors":"W. Wijanarka, Maulida Aqlia, K. Kristina","doi":"10.31957/JBP.485","DOIUrl":null,"url":null,"abstract":"Dahlia bulbs (Dahlia variabilis) contains carbohydrates in the form of inulin. Inulin is a form of fructose polymer from fructose monomers. Inulin hydrolysis produces a product in the form of fructose.Inulinase enzyme is an enzyme able to purely hydrolyze inulin. This study aims to determine the activity of inulinase enzymes and the specific growth rate of IS_1 bacterial isolates producing inulinase in medium of Dahlia tuber flour. Isolates of inulinase-producing bacteria were isolated directly from decay dahlia tubers and used as an inoculum in creating starter.The measurement of cell growth was carried out by inoculating a 20-hour starter on the production medium. Incubation is done for 24 hours using a rotary shaker with a speed of 120 rpm. Sampling was carried out every 4 hours at 0-hour (T0), 4 hours (T4), 8 hours (T8), 12 hours (T12), 16 hours (T16), 20 hours (T20) and 24 hours (T24) intervals with a sample of 5 mL measured for absorbance of λ 520 nm using spectrophotometer. Production medium culture in each sample was taken 1 mL and centrifuged at 3000 rpm for 10 minutes to obtain supernatant of crude enzyme. Measurement of inulinase enzyme activity was carried out using 3,5-dinitrosalicylic acid (DNS) method and spectrophotometric method at λ 570 nm. IS_1 bacterial isolate showed optimum growth at incubation time of 8 hours with OD of 0.647 and had a specific growth rate (µ) of 0.02 / hour with a generation time of 34.65 hours. The highest enzyme activity produced by IS_1 bacteria at 8 hours incubation time was 0.490 IU. The conclusion of this study is that IS_1 bacteria indicates good growth in medium of dahlia tuber flour and has inulinase enzyme activity which is able to hydrolyze inulin into fructose.  Key words: inulin, bacterial isolate, inulinase, production ","PeriodicalId":338791,"journal":{"name":"JURNAL BIOLOGI PAPUA","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JURNAL BIOLOGI PAPUA","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31957/JBP.485","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Dahlia bulbs (Dahlia variabilis) contains carbohydrates in the form of inulin. Inulin is a form of fructose polymer from fructose monomers. Inulin hydrolysis produces a product in the form of fructose.Inulinase enzyme is an enzyme able to purely hydrolyze inulin. This study aims to determine the activity of inulinase enzymes and the specific growth rate of IS_1 bacterial isolates producing inulinase in medium of Dahlia tuber flour. Isolates of inulinase-producing bacteria were isolated directly from decay dahlia tubers and used as an inoculum in creating starter.The measurement of cell growth was carried out by inoculating a 20-hour starter on the production medium. Incubation is done for 24 hours using a rotary shaker with a speed of 120 rpm. Sampling was carried out every 4 hours at 0-hour (T0), 4 hours (T4), 8 hours (T8), 12 hours (T12), 16 hours (T16), 20 hours (T20) and 24 hours (T24) intervals with a sample of 5 mL measured for absorbance of λ 520 nm using spectrophotometer. Production medium culture in each sample was taken 1 mL and centrifuged at 3000 rpm for 10 minutes to obtain supernatant of crude enzyme. Measurement of inulinase enzyme activity was carried out using 3,5-dinitrosalicylic acid (DNS) method and spectrophotometric method at λ 570 nm. IS_1 bacterial isolate showed optimum growth at incubation time of 8 hours with OD of 0.647 and had a specific growth rate (µ) of 0.02 / hour with a generation time of 34.65 hours. The highest enzyme activity produced by IS_1 bacteria at 8 hours incubation time was 0.490 IU. The conclusion of this study is that IS_1 bacteria indicates good growth in medium of dahlia tuber flour and has inulinase enzyme activity which is able to hydrolyze inulin into fructose.  Key words: inulin, bacterial isolate, inulinase, production 
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
大丽亚块茎淀粉中属e -1细菌异位异位的活性和异位异位异位的生长速率
大丽花球茎(Dahlia variabilis)含有菊粉形式的碳水化合物。菊粉是果糖单体的一种果糖聚合物。菊粉水解产生果糖形式的产物。菊粉酶是一种能够纯水解菊粉的酶。本研究旨在测定产菊粉酶的IS_1菌株在大丽花块茎粉培养基中菊粉酶活性和比生长率。从腐烂的大丽花块茎中直接分离出菊粉酶产生菌,并将其作为发酵剂接种。通过在生产培养基上接种20小时的发酵剂来测量细胞的生长。使用转速为120转/分钟的旋转激振器孵育24小时。在0小时(T0)、4小时(T4)、8小时(T8)、12小时(T12)、16小时(T16)、20小时(T20)和24小时(T24)的间隔每4小时取样一次,取5 mL样品,用分光光度计测定λ 520 nm吸光度。每个样品取1 mL生产培养基培养液,在3000 rpm下离心10分钟,得到粗酶上清。采用3,5-二硝基水杨酸(DNS)法和λ 570 nm分光光度法测定菊粉酶活性。IS_1菌株在培养8 h时生长最佳,OD值为0.647,比生长率(µ)为0.02 / h,代时间为34.65 h。IS_1菌在培养8 h时产生的酶活性最高,为0.490 IU。本研究的结论是,IS_1菌在大丽花块茎粉培养基中生长良好,具有将菊粉水解成果糖的菊粉酶活性。关键词:菊粉;分离菌;菊粉酶
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Karakteristik Morfofungsi Skelet Ekstremitas Kaki Soa Layar (Hydrosaurus amboinensis) Keragaman Fenetik Pisang Lokal yang Dimanfaatkan oleh Masyarakat Sentani Kabupaten Jayapura, Papua Studi Etnobotani Pulau Enggano, Provinsi Bengkulu Status Mutu Kualitas Udara Ambien Pada Beberapa Kota Besar di Papua Menggunakan ArcGIS Monitoring Keanekaragaman dan Kemelimpahan Katak dan Kodok (Amphibia: Anura) di Sisi Timur Area Kampus UGM Yogyakarta
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1