Literature DB >> 18951544

Engineering of the alpha-amylase from Geobacillus stearothermophilus US100 for detergent incorporation.

Bassem Khemakhem1, Mamdouh Ben Ali, Nushin Aghajari, Michel Juy, Richard Haser, Samir Bejar.   

Abstract

AmyUS100DeltaIG is a variant of the most thermoactive and thermostable maltohexaose forming alpha-amylase produced by Geobacillus stearothermophilus sp.US100. This enzyme which was designed to improve the thermostability of the wild-type enzyme has acquired a very high resistance to chelator agents. According to modeling structural studies and with the aim of enhancing its resistance towards chemical oxidation, a mutant (AmyUS100DeltaIG/M197A) was created by substituting methionine 197 to alanine. The catalytic proprieties of the resulting mutant show alterations in the specific activity and the profile of starch hydrolysis. Interestingly, AmyUS100DeltaIG/M197A displayed the highest resistance to oxidation compared to the AmyUS100DeltaIG and to Termamyl300, the well-known commercial amylase used in detergent. Further, performance of the engineered alpha-amylase was estimated in the presence of commonly used detergent compounds and a wide range of commercial detergent (liquid and solid). These studies indicated a high compatibility and performance of AmyUS100DeltaIG/M197A, suggesting its potential application in detergent industry.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 18951544     DOI: 10.1002/bit.22083

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  14 in total

1.  A chimeric α-amylase engineered from Bacillus acidicola and Geobacillus thermoleovorans with improved thermostability and catalytic efficiency.

Authors:  Deepak Parashar; T Satyanarayana
Journal:  J Ind Microbiol Biotechnol       Date:  2016-01-20       Impact factor: 3.346

2.  Integrating terminal truncation and oligopeptide fusion for a novel protein engineering strategy to improve specific activity and catalytic efficiency: alkaline α-amylase as a case study.

Authors:  Haiquan Yang; Long Liu; Hyun-dong Shin; Rachel R Chen; Jianghua Li; Guocheng Du; Jian Chen
Journal:  Appl Environ Microbiol       Date:  2013-08-16       Impact factor: 4.792

3.  Engineered glucose isomerase from Streptomyces sp. SK is resistant to Ca²⁺ inhibition and Co²⁺ independent.

Authors:  Hajer Ben Hlima; Nushin Aghajari; Mamdouh Ben Ali; Richard Haser; Samir Bejar
Journal:  J Ind Microbiol Biotechnol       Date:  2011-12-04       Impact factor: 3.346

4.  Cloning and expression of acidstable, high maltose-forming, Ca2+-independent α-amylase from an acidophile Bacillus acidicola and its applicability in starch hydrolysis.

Authors:  Archana Sharma; T Satyanarayana
Journal:  Extremophiles       Date:  2012-04-18       Impact factor: 2.395

5.  Fusion of an oligopeptide to the N terminus of an alkaline α-amylase from Alkalimonas amylolytica simultaneously improves the enzyme's catalytic efficiency, thermal stability, and resistance to oxidation.

Authors:  Haiquan Yang; Xinyao Lu; Long Liu; Jianghua Li; Hyun-dong Shin; Rachel R Chen; Guocheng Du; Jian Chen
Journal:  Appl Environ Microbiol       Date:  2013-03-01       Impact factor: 4.792

6.  Production of Ca2+-Independent and Acidstable Recombinant α-Amylase of Bacillus acidicola Extracellularly and its Applicability in Generating Maltooligosaccharides.

Authors:  Deepak Parashar; T Satyanarayana
Journal:  Mol Biotechnol       Date:  2016-11       Impact factor: 2.695

7.  Structure-based engineering of methionine residues in the catalytic cores of alkaline amylase from Alkalimonas amylolytica for improved oxidative stability.

Authors:  Haiquan Yang; Long Liu; Mingxing Wang; Jianghua Li; Nam Sun Wang; Guocheng Du; Jian Chen
Journal:  Appl Environ Microbiol       Date:  2012-08-03       Impact factor: 4.792

8.  Overproduction of Bacillus amyloliquefaciens extracellular glutamyl-endopeptidase as a result of ectopic multi-copy insertion of an efficiently-expressed mpr gene into the Bacillus subtilis chromosome.

Authors:  Yurgis Av Yomantas; Elena G Abalakina; Lyubov I Golubeva; Lyubov Y Gorbacheva; Sergey V Mashko
Journal:  Microb Cell Fact       Date:  2011-08-05       Impact factor: 5.328

9.  Structure-guided systems-level engineering of oxidation-prone methionine residues in catalytic domain of an alkaline α-amylase from Alkalimonas amylolytica for significant improvement of both oxidative stability and catalytic efficiency.

Authors:  Haiquan Yang; Long Liu; Hyun-dong Shin; Jianghua Li; Guocheng Du; Jian Chen
Journal:  PLoS One       Date:  2013-03-15       Impact factor: 3.240

10.  Native to designed: microbial -amylases for industrial applications.

Authors:  Si Jie Lim; Siti Nurbaya Oslan
Journal:  PeerJ       Date:  2021-05-18       Impact factor: 2.984

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.