Literature DB >> 11150607

Protein engineering of subtilisin.

P N Bryan1.   

Abstract

The serine protease subtilisin is an important industrial enzyme as well as a model for understanding the enormous rate enhancements affected by enzymes. For these reasons along with the timely cloning of the gene, ease of expression and purification and availability of atomic resolution structures, subtilisin became a model system for protein engineering studies in the 1980s. Fifteen years later, mutations in well over 50% of the 275 amino acids of subtilisin have been reported in the scientific literature. Most subtilisin engineering has involved catalytic amino acids, substrate binding regions and stabilizing mutations. Stability has been the property of subtilisin which has been most amenable to enhancement, yet perhaps least understood. This review will give a brief overview of the subtilisin engineering field, critically review what has been learned about subtilisin stability from protein engineering experiments and conclude with some speculation about the prospects for future subtilisin engineering.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11150607     DOI: 10.1016/s0167-4838(00)00235-1

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  34 in total

1.  Cloning of a fibrinolytic enzyme (subtilisin) gene from Bacillus subtilis in Escherichia coli.

Authors:  Younes Ghasemi; Fatemeh Dabbagh; Abdollah Ghasemian
Journal:  Mol Biotechnol       Date:  2012-09       Impact factor: 2.695

2.  Ca2+-dependent maturation of subtilisin from a hyperthermophilic archaeon, Thermococcus kodakaraensis: the propeptide is a potent inhibitor of the mature domain but is not required for its folding.

Authors:  Marian Pulido; Kenji Saito; Shun-Ichi Tanaka; Yuichi Koga; Masaaki Morikawa; Kazufumi Takano; Shigenori Kanaya
Journal:  Appl Environ Microbiol       Date:  2006-06       Impact factor: 4.792

Review 3.  Laboratory-directed protein evolution.

Authors:  Ling Yuan; Itzhak Kurek; James English; Robert Keenan
Journal:  Microbiol Mol Biol Rev       Date:  2005-09       Impact factor: 11.056

Review 4.  Lessons in stability from thermophilic proteins.

Authors:  Abbas Razvi; J Martin Scholtz
Journal:  Protein Sci       Date:  2006-07       Impact factor: 6.725

5.  Purification and characterization of a fibrinolytic subtilisin-like protease of Bacillus subtilis TP-6 from an Indonesian fermented soybean, Tempeh.

Authors:  Seong-Bo Kim; Dong-Woo Lee; Chan-Ick Cheigh; Eun-Ah Choe; Sang-Jae Lee; Young-Ho Hong; Hak-Jong Choi; Yu-Ryang Pyun
Journal:  J Ind Microbiol Biotechnol       Date:  2006-02-10       Impact factor: 3.346

6.  Probing the importance of hydrogen bonds in the active site of the subtilisin nattokinase by site-directed mutagenesis and molecular dynamics simulation.

Authors:  Zhong-liang Zheng; Mao-qing Ye; Zhen-yu Zuo; Zhi-gang Liu; Keng-chang Tai; Guo-lin Zou
Journal:  Biochem J       Date:  2006-05-01       Impact factor: 3.857

7.  Engineering protease specificity made simple, but not simpler.

Authors:  Enrico Di Cera
Journal:  Nat Chem Biol       Date:  2008-05       Impact factor: 15.040

8.  SOD1 exhibits allosteric frustration to facilitate metal binding affinity.

Authors:  Atanu Das; Steven S Plotkin
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-19       Impact factor: 11.205

9.  Types and effects of protein variations.

Authors:  Mauno Vihinen
Journal:  Hum Genet       Date:  2015-01-24       Impact factor: 4.132

10.  Engineering and directed evolution of a Ca2+ binding site A-deficient AprE mutant reveal an essential contribution of the loop Leu75-Leu82 to enzyme activity.

Authors:  Eliel R Romero-García; Alfredo Téllez-Valencia; María F Trujillo; José G Sampedro; Hugo Nájera; Arturo Rojo-Domínguez; Jesús García-Soto; Mario Pedraza-Reyes
Journal:  J Biomed Biotechnol       Date:  2009-08-20
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.