Expression of β-glucanase Gene from Bacillus macerans in Escherichia coli

The β-glucanase gene from recombined cloning plasmid was subcloned into BamH Ⅰ and Xho Ⅰsite of expression plasmid pET-30a. The recombined expression plasmid was transformed into Escherichia coli strain BL21. The result of SDS-PAGE showed that about 25.0 kD protein of β-1, 3-1,4-glucanase was expres...

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Main Authors: LI Wei-fen, YAO Jiang-tao, HU Chun-xia, XU Zi-rong
Format: Article
Language:English
Published: Zhejiang University Press 2005-09-01
Series:浙江大学学报. 农业与生命科学版
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Online Access:https://www.academax.com/doi/10.3785/1008-9209.2005.05.0628
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author LI Wei-fen
YAO Jiang-tao
HU Chun-xia
XU Zi-rong
author_facet LI Wei-fen
YAO Jiang-tao
HU Chun-xia
XU Zi-rong
author_sort LI Wei-fen
collection DOAJ
description The β-glucanase gene from recombined cloning plasmid was subcloned into BamH Ⅰ and Xho Ⅰsite of expression plasmid pET-30a. The recombined expression plasmid was transformed into Escherichia coli strain BL21. The result of SDS-PAGE showed that about 25.0 kD protein of β-1, 3-1,4-glucanase was expressed in E. coli strain BL21 containing recombined plasmid. The enzyme activity of the recombinant was 60.4 U/mL, which was about 30-fold higher than that of the original strain. The optimal temperature and pH of the enzyme were 50℃ and 5.0-7.0, respectively. The enzyme was relatively stable at temperature below 50℃ for 2 min, and almost unaffected after 60min between pH 3.0 and 9.0.
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issn 1008-9209
2097-5155
language English
publishDate 2005-09-01
publisher Zhejiang University Press
record_format Article
series 浙江大学学报. 农业与生命科学版
spelling doaj-art-caf86e76f8c8444a922b09983aa7211f2025-08-20T03:58:19ZengZhejiang University Press浙江大学学报. 农业与生命科学版1008-92092097-51552005-09-013162863210.3785/1008-9209.2005.05.062810089209Expression of β-glucanase Gene from Bacillus macerans in Escherichia coliLI Wei-fenYAO Jiang-taoHU Chun-xiaXU Zi-rongThe β-glucanase gene from recombined cloning plasmid was subcloned into BamH Ⅰ and Xho Ⅰsite of expression plasmid pET-30a. The recombined expression plasmid was transformed into Escherichia coli strain BL21. The result of SDS-PAGE showed that about 25.0 kD protein of β-1, 3-1,4-glucanase was expressed in E. coli strain BL21 containing recombined plasmid. The enzyme activity of the recombinant was 60.4 U/mL, which was about 30-fold higher than that of the original strain. The optimal temperature and pH of the enzyme were 50℃ and 5.0-7.0, respectively. The enzyme was relatively stable at temperature below 50℃ for 2 min, and almost unaffected after 60min between pH 3.0 and 9.0.https://www.academax.com/doi/10.3785/1008-9209.2005.05.0628β-glucanase<italic>Bacillus macerans</italic><italic>Escherichia coli</italic>expressionenzymatic properties
spellingShingle LI Wei-fen
YAO Jiang-tao
HU Chun-xia
XU Zi-rong
Expression of β-glucanase Gene from Bacillus macerans in Escherichia coli
浙江大学学报. 农业与生命科学版
β-glucanase
<italic>Bacillus macerans</italic>
<italic>Escherichia coli</italic>
expression
enzymatic properties
title Expression of β-glucanase Gene from Bacillus macerans in Escherichia coli
title_full Expression of β-glucanase Gene from Bacillus macerans in Escherichia coli
title_fullStr Expression of β-glucanase Gene from Bacillus macerans in Escherichia coli
title_full_unstemmed Expression of β-glucanase Gene from Bacillus macerans in Escherichia coli
title_short Expression of β-glucanase Gene from Bacillus macerans in Escherichia coli
title_sort expression of β glucanase gene from bacillus macerans in escherichia coli
topic β-glucanase
<italic>Bacillus macerans</italic>
<italic>Escherichia coli</italic>
expression
enzymatic properties
url https://www.academax.com/doi/10.3785/1008-9209.2005.05.0628
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AT yaojiangtao expressionofbglucanasegenefrombacillusmaceransinescherichiacoli
AT huchunxia expressionofbglucanasegenefrombacillusmaceransinescherichiacoli
AT xuzirong expressionofbglucanasegenefrombacillusmaceransinescherichiacoli