Stepwise optimization of a low-temperature Bacillus subtilis expression system for "difficult to express” proteins

Verfasser / Beitragende:
[Norma Welsch, Georg Homuth, Thomas Schweder]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Microbiology and Biotechnology, 99/15(2015-08-01), 6363-6376
Format:
Artikel (online)
ID: 605506752
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024 7 0 |a 10.1007/s00253-015-6552-y  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00253-015-6552-y 
245 0 0 |a Stepwise optimization of a low-temperature Bacillus subtilis expression system for "difficult to express” proteins  |h [Elektronische Daten]  |c [Norma Welsch, Georg Homuth, Thomas Schweder] 
520 3 |a In order to improve the overproduction of "difficult to express” proteins, a low-temperature expression system for Bacillus subtilis based on the cold-inducible promoter of the desaturase-encoding des gene was constructed. Selected regulatory DNA sequence elements from B. subtilis genes known to be cold-inducible were fused to different model genes. It could be demonstrated that these regulatory elements are able to mediate increased heterologous gene expression, either by improved translation efficiency or by higher messenger RNA (mRNA) stability. In case of a cold-adapted β-galactosidase from Pseudoalteromonas haloplanktis TAE79A serving as the model, significantly higher expression was achieved by fusing its coding sequence to the so-called "downstream box” sequence of cspB encoding the major B. subtilis cold-shock protein. The combination of this fusion with a cspB 5′-UTR stem-loop structure resulted in further enhancement of the β-galactosidase expression. In addition, integration of the transcription terminator of the B. subtilis cold-inducible bkd operon downstream of the target genes caused a higher mRNA stability and enabled thus a further significant increase in expression. Finally, the fully optimized expression system was validated by overproducing a B. subtilis xylanase as well as an α-glucosidase from Saccharomyces cerevisiae, the latter known for tending to form inclusion bodies. These analyses verified the applicability of the engineered expression system for extracellular and intracellular protein synthesis in B. subtilis, thereby confirming the suitability of this host organism for the overproduction of critical, poorly soluble proteins. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Bacillus subtilis  |2 nationallicence 
690 7 |a Recombinant low-temperature expression  |2 nationallicence 
690 7 |a Overproduction of insoluble proteins  |2 nationallicence 
690 7 |a Cold induction  |2 nationallicence 
700 1 |a Welsch  |D Norma  |u Pharmaceutical Biotechnology, Institute of Pharmacy, Ernst-Moritz-Arndt-University, Felix-Hausdorff-Str. 3, 17487, Greifswald, Germany  |4 aut 
700 1 |a Homuth  |D Georg  |u Interfaculty Institute for Genetics and Functional Genomics, Department of Functional Genomics, University Medicine and Ernst-Moritz-Arndt University Greifswald, Friedrich-Ludwig-Jahn-Str. 15 a, 17487, Greifswald, Germany  |4 aut 
700 1 |a Schweder  |D Thomas  |u Pharmaceutical Biotechnology, Institute of Pharmacy, Ernst-Moritz-Arndt-University, Felix-Hausdorff-Str. 3, 17487, Greifswald, Germany  |4 aut 
773 0 |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/15(2015-08-01), 6363-6376  |x 0175-7598  |q 99:15<6363  |1 2015  |2 99  |o 253 
856 4 0 |u https://doi.org/10.1007/s00253-015-6552-y  |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/s00253-015-6552-y  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Welsch  |D Norma  |u Pharmaceutical Biotechnology, Institute of Pharmacy, Ernst-Moritz-Arndt-University, Felix-Hausdorff-Str. 3, 17487, Greifswald, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Homuth  |D Georg  |u Interfaculty Institute for Genetics and Functional Genomics, Department of Functional Genomics, University Medicine and Ernst-Moritz-Arndt University Greifswald, Friedrich-Ludwig-Jahn-Str. 15 a, 17487, Greifswald, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Schweder  |D Thomas  |u Pharmaceutical Biotechnology, Institute of Pharmacy, Ernst-Moritz-Arndt-University, Felix-Hausdorff-Str. 3, 17487, Greifswald, Germany  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/15(2015-08-01), 6363-6376  |x 0175-7598  |q 99:15<6363  |1 2015  |2 99  |o 253