High‐level expression and characterization of a new κ‐carrageenase from marine bacterium Pedobacter hainanensis NJ‐02. (9th March 2018)
- Record Type:
- Journal Article
- Title:
- High‐level expression and characterization of a new κ‐carrageenase from marine bacterium Pedobacter hainanensis NJ‐02. (9th March 2018)
- Main Title:
- High‐level expression and characterization of a new κ‐carrageenase from marine bacterium Pedobacter hainanensis NJ‐02
- Authors:
- Zhu, B.‐W.
Xiong, Q.
Ni, F.
Sun, Y.
Yao, Z. - Abstract:
- Abstract: A novel κ ‐carrageenase gene ( CgkB ) has been cloned from Pedobacter hainanensis NJ‐02 and expressed heterologously in Escherichia coli BL21 (DE3). It consisted of 1935 bp and encoded 644 amino acid residues with a molecular weight of 71·61 kDa. The recombinant enzyme showed maximal activity of 2458 U mg −1 at 40°C and pH 8·0. Additionally, it could retain more than 70% of its maximal activity after being incubated at pH of 5·5–10·0 below 40°C. K + and a broad range of NaCl can activate the enzyme. The K m and V max of CgkB was 2·4 mg ml −1 and 126 mmol mg −1 min −1 . The ESI‐MS analysis of hydrolysates indicated that the enzyme can endolytically depolymerize the carrageenan into tetrasaccharides and hexasaccharides. The results indicated that the enzyme with high activity could be a valuable enzyme tool to produce carrageenan oligosaccharides with various activities. Significance and Impact of the Study: Enzymatic preparation of carrageenan oligosaccharides has drawn increased attention due to their various physiological activities. It is urgent to explore enzyme tools with higher activity and better stability. In this work, a novel κ ‐carrageenase was identified and characterized from marine bacterium Pedobacter hainanensis NJ‐02. The enzyme with high activity could be a valuable tool to produce carrageenan oligosaccharides with various activities Abstract : Significance and Impact of the Study: Enzymatic preparation of carrageenan oligosaccharides has drawnAbstract: A novel κ ‐carrageenase gene ( CgkB ) has been cloned from Pedobacter hainanensis NJ‐02 and expressed heterologously in Escherichia coli BL21 (DE3). It consisted of 1935 bp and encoded 644 amino acid residues with a molecular weight of 71·61 kDa. The recombinant enzyme showed maximal activity of 2458 U mg −1 at 40°C and pH 8·0. Additionally, it could retain more than 70% of its maximal activity after being incubated at pH of 5·5–10·0 below 40°C. K + and a broad range of NaCl can activate the enzyme. The K m and V max of CgkB was 2·4 mg ml −1 and 126 mmol mg −1 min −1 . The ESI‐MS analysis of hydrolysates indicated that the enzyme can endolytically depolymerize the carrageenan into tetrasaccharides and hexasaccharides. The results indicated that the enzyme with high activity could be a valuable enzyme tool to produce carrageenan oligosaccharides with various activities. Significance and Impact of the Study: Enzymatic preparation of carrageenan oligosaccharides has drawn increased attention due to their various physiological activities. It is urgent to explore enzyme tools with higher activity and better stability. In this work, a novel κ ‐carrageenase was identified and characterized from marine bacterium Pedobacter hainanensis NJ‐02. The enzyme with high activity could be a valuable tool to produce carrageenan oligosaccharides with various activities Abstract : Significance and Impact of the Study: Enzymatic preparation of carrageenan oligosaccharides has drawn increased attention due to their various physiological activities. It is urgent to explore enzyme tools with higher activity and better stability. In this work, a novel κ ‐carrageenase was identified and characterized from marine bacterium Pedobacter hainanensis NJ‐02. The enzyme with high activity could be a valuable tool to produce carrageenan oligosaccharides with various activities. … (more)
- Is Part Of:
- Letters in applied microbiology. Volume 66:Number 5(2018)
- Journal:
- Letters in applied microbiology
- Issue:
- Volume 66:Number 5(2018)
- Issue Display:
- Volume 66, Issue 5 (2018)
- Year:
- 2018
- Volume:
- 66
- Issue:
- 5
- Issue Sort Value:
- 2018-0066-0005-0000
- Page Start:
- 409
- Page End:
- 415
- Publication Date:
- 2018-03-09
- Subjects:
- carrageenase -- characterization -- cloning -- expression -- oligosaccharides
Microbiology -- Periodicals
660.62 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1472-765X ↗
https://academic.oup.com/lambio ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/lam.12865 ↗
- Languages:
- English
- ISSNs:
- 0266-8254
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5185.126700
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6343.xml