Excretory over-expression of Bacillus sp. G1 cyclodextrin glucanotransferase (CGTase) in Escherichia coli: Optimization of the cultivation conditions by response surface methodology

Enzyme and Microbial Technology

Volumn 40, Issue 5, 2007, Pages 1256-1263

  Lo, Po Kim ^a   Hassan, Osman ^b   Ahmad, Arshad ^a   Mahadi, Nor Muhammad ^b   Illias, Rosli Md ^a  

^a UNIVERSITI TEKNOLOGI MALAYSIA   (Malaysia)

^b UNIVERSITI KEBANGSAAN MALAYSIA   (Malaysia)

Author keywords

E. coli; Extracellular; Optimization; Recombinant CGTase; RSM

Indexed keywords

CELLS; CYCLODEXTRINS; ESCHERICHIA COLI; OPTIMIZATION;

CYCLODEXTRIN GLUCANOTRANSFERASE (CGTASE); EXTRACELLULAR RECOMBINANT CGTASE ACTIVITY; POST-INDUCTION TEMPERATURE; RECOMBINANT CGTASE; RESPONSE SURFACE METHODOLOGY;

ENZYME ACTIVITY;

BACTERIAL ENZYME; BACTERIOCIN; CYCLOMALTODEXTRIN GLUCANOTRANSFERASE;

ARTICLE; BACILLUS; CGT GENE; ENZYME ANALYSIS; ESCHERICHIA COLI; GENE ISOLATION; GENE OVEREXPRESSION; NONHUMAN; PROCESS DESIGN; REACTION OPTIMIZATION; RESPONSE SURFACE METHOD; SPECIES CULTIVATION;

BACILLUS SP.; ESCHERICHIA COLI;

EID: 33847625491     PISSN: 01410229     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.enzmictec.2006.09.020     Document Type: Article

References (22)

1. Pishtiyski I., and Zhekova B. Effect of different substrates and their preliminary treatment on cyclodextrin production. W. J. Microbiol Biotechnol 22 (2006) 109-114
2. Pedersen S., Dijkhuizen L., Dijkstra B.W., Jersen B.F., and Jørgensen S.T. A better enzyme for cyclodextrins. CHEMTECH (1995) 19-25
3. Tao B.Y. Cyclodextrin glucanotransferases: technology and biocatalyst design. American Chemical Society: Enzyme in biomass conversion (1991), American Chemical Society, WDC p. 372-83
4. Kimura K., Takano T., and Tamane K. Molecular cloning of the β-cyclodextrin synthetase gene from an alkalophilic Bacillus and its expression in Escherichia coli and Bacillus subtilis. Appl Microbiol Biotechnol 26 (1987) 149-153
5. Nam S.W., Park H.Y., Kim J.H., Seo J.H., Han N.S., and Kim B.W. Expression of Bacillus macerans cyclodextrin glucanotransferase gene in Sacchoromyces cerevisiae. Biotechnol Lett 23 (2001) 730-772
6. Kim S.G., Kweon D.H., Lee D.H., Park Y.C., and Seo J.H. Coexpression of folding accessory proteins for production of active cyclodextrin glycosyltransferase of Bacillus macerans in recombinant Escherichia coli. Protein Expr Purif 41 (2005) 426-432
7. Kim C.I., Kim M.D., and Park Y.C. Refolding of Bacillus macerans cyclodextrin glucanotransferase expressed as inclusion bodies in recombinant Escherichia coli. J Microbiol Biotechnol 10 (2000) 632-637
8. Lee K.C.P., and Tao B. High-level expression of cyclodextrin glycosyltransferase in E. coli using a T7 promoter expression system. Starch 46 (1994) 67-74
9. Miller J.H. Experiments In Molecular Genetic (1972), Cold Spring Harbor Laboratory, Cold Spring Harbor, New York
10. Kaneko T., Kato T., Nakamura N., and Horikhoshi K. Spectrophotometric determination of cyclozation activity of β-cyclodextrin-forming cyclodextrin glucanotransferase. J. Jpn Soc Starch Sci 34 (1987) 45-48
11. Myers M., and Montgomery D.C. Response surface methodology: process and product optimization using designed experiments (2002), John Wiley and Sons, USA
12. Mergulhão F.J.M., Summers D.K., and Monteiro G.A. Recombinant protein secretion in Escherichia coli. Biotechnol Adv 23 (2005) 177-202
13. Shokri A., Sanden M., and Larsson G. Cell and process design for targeting of recombinant protein into the culture medium of Escherichia coli. Appl Microbiol Biotechnol 60 (2003) 654-664
14. Van der Wal F.J., Luirink J., and Oudega B. Bacteriocin release protein: mode of action, structure, and biotechnological application. FEMS Microbiol Rev 17 (1995) 381-399
15. Wang Y.H., Jing C.F., Yang B., Mainda G., Dong M.L., and Xu A.L. Production of a new sea anemone neurotoxin by recombinant Escherichia coli: optimization of culture conditions using response surface methodology. Process Biochem 40 (2005) 2721-2728
16. León A.D., Islas H.J., Cuevas M.G., and Rosa A.P.B. Analysis of the expression of the Trichoderma harzianum ech42 gene in two isogenic clones of Escherichia coli by surface response methodology. Process Biochem 39 (2004) 2173-2178
17. Villaverde A., and Carrió M.M. Protein aggregation in recombinant bacteria: biological role of inclusion bodies. Biotechnol Lett 25 (2003) 1385-1395
18. Schein C.H. Production of soluble recombinant protein in bacteria. Biotechnology 7 (1989) 1141-1149
19. Fu Z., Hamid S.A., Razak C.N.A., Basri M., Salleh A.B., and Rahman R.N.Z. Secretory expression in Escherichia coli and single-step purification of a heat-stable alkaline protease. Protein Expr Purif 28 (2003) 63-68
20. Sunitha K., Kim Y.O., Lee J.K., and Oh T.K. Statistical optimization of seed and induction conditions to enhance phytase production by recombinant Escherichia coli. Biochem Eng. J 5 (2000) 51-56
21. Wong T.E., Illias R.M., Salleh M.M., Hassan O., Kamaruddin K., Rahman R.A., et al. Initial screening of fermentation variables for the production of cyclodextrin glucanotransferase (CGTase) from local isolated Bacillus stearothermophillus HR1. Dev Chem Eng Mineral Process 13 5/6 (2005) 1-8
22. Ibrahim H.M., Yusoff W.M.W., Hamid A.A., Illias R.M., Hassan O., and Omar O. Optimization of medium for the production of β-cyclodextrin glucanotransferase using central composite design (CCD). Process Biochem 40 (2005) 753-758