Identifikasi Gen 16S rRNA Bakteri Asam Laktat UBC-DTK-01 dari Dadih

Azizah Azizah, Minda Azhar
{"title":"Identifikasi Gen 16S rRNA Bakteri Asam Laktat UBC-DTK-01 dari Dadih","authors":"Azizah Azizah, Minda Azhar","doi":"10.24036/p.v11i2.113724","DOIUrl":null,"url":null,"abstract":"— Genotypic identification of bacteria is faster than phenotypic identification. This study aims to determine the group of lactic acid bacteria species from Tilatang Kamang Agam curd using the 16S rRNA gene. Bacterial chromosomal DNA was isolated using the kit wizard genomic DNA purification method. The 16S rRNA gene in chromosomal DNA was isolated by PCR method using BacF1 and UniB1 primers. The 16S rRNA gene fragment sequencing was carried out using the Dideoxy Sanger method. The sequenced nucleotide base sequences were analyzed using the BioEdit, BLASTn and MEGA X programs. The size of the 16S rRNA gene fragment of the bacterial isolate UBC-DTK-01 obtained was 1017 bp (base pair). The bacterial isolates belonged to the Enterococcus genus and Enterococcus faecalis species strain UBC-DTK-01.","PeriodicalId":213875,"journal":{"name":"Jurnal Periodic Jurusan Kimia UNP","volume":"33 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jurnal Periodic Jurusan Kimia UNP","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.24036/p.v11i2.113724","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

— Genotypic identification of bacteria is faster than phenotypic identification. This study aims to determine the group of lactic acid bacteria species from Tilatang Kamang Agam curd using the 16S rRNA gene. Bacterial chromosomal DNA was isolated using the kit wizard genomic DNA purification method. The 16S rRNA gene in chromosomal DNA was isolated by PCR method using BacF1 and UniB1 primers. The 16S rRNA gene fragment sequencing was carried out using the Dideoxy Sanger method. The sequenced nucleotide base sequences were analyzed using the BioEdit, BLASTn and MEGA X programs. The size of the 16S rRNA gene fragment of the bacterial isolate UBC-DTK-01 obtained was 1017 bp (base pair). The bacterial isolates belonged to the Enterococcus genus and Enterococcus faecalis species strain UBC-DTK-01.
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
确认rRNA基因16是乳酸UBC-DTK-01的抗凝血剂
-细菌的基因型鉴定比表型鉴定快。本研究旨在利用16S rRNA基因对Tilatang Kamang Agam凝乳中的乳酸菌进行类群鉴定。采用试剂盒向导基因组DNA纯化方法分离细菌染色体DNA。利用BacF1和UniB1引物,采用PCR方法分离染色体DNA中的16S rRNA基因。16S rRNA基因片段测序采用Dideoxy Sanger法。测序后的核苷酸碱基序列使用BioEdit、BLASTn和MEGA X程序进行分析。得到的细菌分离物UBC-DTK-01的16S rRNA基因片段大小为1017 bp(碱基对)。分离的细菌属于肠球菌属和粪肠球菌属UBC-DTK-01菌株。
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
Pengaruh pH dan Konsentrasi Terhadap Penyerapan Ion Logam Pb2+ Menggunakan Kulit Buah Matoa (Pometia pinnata) Degradasi Zat Warna Indigosol Red Ir Menggunakan Metode Sonolisis Dengan Bantuan Katalis ZnO Analisis Proksimat Karbon Ampas Bengkuang (Pachyrhzus erosus) sebagai Sumber Material Maju Uji Kondisi Optimum Desorpsi Anion Fosfat pada Silika Mesopori Termodifikasi DMA (Dimethylamine) Pengaruh Penambahan Carboxymethyl Cellulose (CMC) Terhadap Sifat Mekanik Dan Biodegradasi Plastik Biodegradable Berbasis Selulosa Bakteri –Polietilen Glikol (PEG) Dari Air Kelapa (Cocos nucifera)
×
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