Cargando…

Isolation, identification, and whole-genome sequencing of high-yield protease bacteria from Daqu of ZhangGong Laojiu

A total of 296 strains of protease-producing bacteria were isolated and purified from medium-temperature Daqu produced by ZhangGong LaoJiu Wine Co. Ltd. After calculating the ratio of transparent ring diameter to colony diameter and measuring the protease activities, a strain of high-yield protease...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Yanbo, Fu, Junying, Wang, Linlin, Zhao, Zhijun, Wang, Huihui, Han, Suna, Sun, Xiyu, Pan, Chunmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041807/
https://www.ncbi.nlm.nih.gov/pubmed/35472204
http://dx.doi.org/10.1371/journal.pone.0264677
_version_ 1784694575616491520
author Liu, Yanbo
Fu, Junying
Wang, Linlin
Zhao, Zhijun
Wang, Huihui
Han, Suna
Sun, Xiyu
Pan, Chunmei
author_facet Liu, Yanbo
Fu, Junying
Wang, Linlin
Zhao, Zhijun
Wang, Huihui
Han, Suna
Sun, Xiyu
Pan, Chunmei
author_sort Liu, Yanbo
collection PubMed
description A total of 296 strains of protease-producing bacteria were isolated and purified from medium-temperature Daqu produced by ZhangGong LaoJiu Wine Co. Ltd. After calculating the ratio of transparent ring diameter to colony diameter and measuring the protease activities, a strain of high-yield protease bacteria, called DW-7, was screened out with a protease activity of 99.54 U/mL. Through morphological observation, 16S rDNA sequence analysis, and physiological and biochemical tests, the isolated bacteria DW-7 was determined to be Bacillus velezensis. In addition, whole-genome sequencing (WGS), using PacBio and the Illumina platform, was performed. Gene annotation was then conducted using the Clusters of Orthologous Groups (COG), Kyoto Encyclopedia of Genes and Genomes (KEGG), Non-Redundant Protein Sequence Database (NR), and Gene Ontology (GO) databases. The results showed that the genome of DW-7 was 3,942,829 bp long with a GC content of 46.45%. A total of 3,662 protein-encoding genes were predicted, with a total length of 3,402,822 bp. Additionally, 2,283; 2,796; and 2,127 genes were annotated in the COG, KEGG, and GO databases, respectively. A total of 196 high-yield protease genes were mainly enriched in the metabolism of alanine, aspartic acid, glutamate, glycine, serine, and threonine, as well as ABC transporter and transporter pathways.
format Online
Article
Text
id pubmed-9041807
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-90418072022-04-27 Isolation, identification, and whole-genome sequencing of high-yield protease bacteria from Daqu of ZhangGong Laojiu Liu, Yanbo Fu, Junying Wang, Linlin Zhao, Zhijun Wang, Huihui Han, Suna Sun, Xiyu Pan, Chunmei PLoS One Research Article A total of 296 strains of protease-producing bacteria were isolated and purified from medium-temperature Daqu produced by ZhangGong LaoJiu Wine Co. Ltd. After calculating the ratio of transparent ring diameter to colony diameter and measuring the protease activities, a strain of high-yield protease bacteria, called DW-7, was screened out with a protease activity of 99.54 U/mL. Through morphological observation, 16S rDNA sequence analysis, and physiological and biochemical tests, the isolated bacteria DW-7 was determined to be Bacillus velezensis. In addition, whole-genome sequencing (WGS), using PacBio and the Illumina platform, was performed. Gene annotation was then conducted using the Clusters of Orthologous Groups (COG), Kyoto Encyclopedia of Genes and Genomes (KEGG), Non-Redundant Protein Sequence Database (NR), and Gene Ontology (GO) databases. The results showed that the genome of DW-7 was 3,942,829 bp long with a GC content of 46.45%. A total of 3,662 protein-encoding genes were predicted, with a total length of 3,402,822 bp. Additionally, 2,283; 2,796; and 2,127 genes were annotated in the COG, KEGG, and GO databases, respectively. A total of 196 high-yield protease genes were mainly enriched in the metabolism of alanine, aspartic acid, glutamate, glycine, serine, and threonine, as well as ABC transporter and transporter pathways. Public Library of Science 2022-04-26 /pmc/articles/PMC9041807/ /pubmed/35472204 http://dx.doi.org/10.1371/journal.pone.0264677 Text en © 2022 Liu et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liu, Yanbo
Fu, Junying
Wang, Linlin
Zhao, Zhijun
Wang, Huihui
Han, Suna
Sun, Xiyu
Pan, Chunmei
Isolation, identification, and whole-genome sequencing of high-yield protease bacteria from Daqu of ZhangGong Laojiu
title Isolation, identification, and whole-genome sequencing of high-yield protease bacteria from Daqu of ZhangGong Laojiu
title_full Isolation, identification, and whole-genome sequencing of high-yield protease bacteria from Daqu of ZhangGong Laojiu
title_fullStr Isolation, identification, and whole-genome sequencing of high-yield protease bacteria from Daqu of ZhangGong Laojiu
title_full_unstemmed Isolation, identification, and whole-genome sequencing of high-yield protease bacteria from Daqu of ZhangGong Laojiu
title_short Isolation, identification, and whole-genome sequencing of high-yield protease bacteria from Daqu of ZhangGong Laojiu
title_sort isolation, identification, and whole-genome sequencing of high-yield protease bacteria from daqu of zhanggong laojiu
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9041807/
https://www.ncbi.nlm.nih.gov/pubmed/35472204
http://dx.doi.org/10.1371/journal.pone.0264677
work_keys_str_mv AT liuyanbo isolationidentificationandwholegenomesequencingofhighyieldproteasebacteriafromdaquofzhanggonglaojiu
AT fujunying isolationidentificationandwholegenomesequencingofhighyieldproteasebacteriafromdaquofzhanggonglaojiu
AT wanglinlin isolationidentificationandwholegenomesequencingofhighyieldproteasebacteriafromdaquofzhanggonglaojiu
AT zhaozhijun isolationidentificationandwholegenomesequencingofhighyieldproteasebacteriafromdaquofzhanggonglaojiu
AT wanghuihui isolationidentificationandwholegenomesequencingofhighyieldproteasebacteriafromdaquofzhanggonglaojiu
AT hansuna isolationidentificationandwholegenomesequencingofhighyieldproteasebacteriafromdaquofzhanggonglaojiu
AT sunxiyu isolationidentificationandwholegenomesequencingofhighyieldproteasebacteriafromdaquofzhanggonglaojiu
AT panchunmei isolationidentificationandwholegenomesequencingofhighyieldproteasebacteriafromdaquofzhanggonglaojiu