Thermostability enhancement of an endo-1,4-β-galactanase from Talaromyces stipitatus by site-directed mutagenesis

Verfasser / Beitragende:
[Dorte Larsen, Christian Nyffenegger, Maria Swiniarska, Anders Thygesen, Mikael Strube, Anne Meyer, Jørn Mikkelsen]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Microbiology and Biotechnology, 99/10(2015-05-01), 4245-4253
Format:
Artikel (online)
ID: 605502315
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024 7 0 |a 10.1007/s00253-014-6244-z  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00253-014-6244-z 
245 0 0 |a Thermostability enhancement of an endo-1,4-β-galactanase from Talaromyces stipitatus by site-directed mutagenesis  |h [Elektronische Daten]  |c [Dorte Larsen, Christian Nyffenegger, Maria Swiniarska, Anders Thygesen, Mikael Strube, Anne Meyer, Jørn Mikkelsen] 
520 3 |a Enzymatic conversion of pectinaceous biomasses such as potato and sugar beet pulp at high temperatures is advantageous as it gives rise to lower substrate viscosity, easier mixing, and increased substrate solubility and lowers the risk of contamination. Such high-temperature processing requires development of thermostable enzymes. Talaromyces stipitatus was found to secrete endo-1,4-β-galactanase when grown on sugar beet pectin as sole carbon source. The mature protein contained 353 AA and the MW was estimated to 36.5kDa. It was subjected to codon optimization and produced in Pichia pastoris in 2l scale yielding 5.3g. The optimal reaction condition for the endo-1,4-β-galactanase was determined to be 46°C at pH4.5 at which the specific activity was estimated to be 6.93μmol/min/mg enzyme with half-lives of 13 and 2min at 55 and 60°C, respectively. For enhancement of the half-life of TSGAL, nine single amino acid residues were selected for site-directed mutagenesis on the basis of semi-rational design. Of these nine mutants, G305A showed half-lives of 114min at 55°C and 15min at 60°C, respectively. This is 8.6-fold higher than that of the TSGAL at 55°C, whereas the other mutants displayed moderate positive to negative changes in their half-lives. 
540 |a Springer-Verlag Berlin Heidelberg, 2014 
690 7 |a Protein engineering  |2 nationallicence 
690 7 |a Semi-rational design  |2 nationallicence 
690 7 |a Multiple alignment  |2 nationallicence 
690 7 |a GH53  |2 nationallicence 
690 7 |a Half-life  |2 nationallicence 
700 1 |a Larsen  |D Dorte  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
700 1 |a Nyffenegger  |D Christian  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
700 1 |a Swiniarska  |D Maria  |u Dako Denmark A/S, Produktionsvej 42, 2600, Glostrup, Denmark  |4 aut 
700 1 |a Thygesen  |D Anders  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
700 1 |a Strube  |D Mikael  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
700 1 |a Meyer  |D Anne  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
700 1 |a Mikkelsen  |D Jørn  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
773 0 |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/10(2015-05-01), 4245-4253  |x 0175-7598  |q 99:10<4245  |1 2015  |2 99  |o 253 
856 4 0 |u https://doi.org/10.1007/s00253-014-6244-z  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00253-014-6244-z  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Larsen  |D Dorte  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Nyffenegger  |D Christian  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Swiniarska  |D Maria  |u Dako Denmark A/S, Produktionsvej 42, 2600, Glostrup, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Thygesen  |D Anders  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Strube  |D Mikael  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Meyer  |D Anne  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Mikkelsen  |D Jørn  |u Center for Bioprocess Engineering, Department of Chemical and Biochemical Engineering, Technical University of Denmark, Building 229, 2800, Kongens Lyngby, Denmark  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/10(2015-05-01), 4245-4253  |x 0175-7598  |q 99:10<4245  |1 2015  |2 99  |o 253