Improvement in the secretory expression of recombinant Candida rugosa lipase in Pichia pastoris. Issue 12 (December 2015)
- Record Type:
- Journal Article
- Title:
- Improvement in the secretory expression of recombinant Candida rugosa lipase in Pichia pastoris. Issue 12 (December 2015)
- Main Title:
- Improvement in the secretory expression of recombinant Candida rugosa lipase in Pichia pastoris
- Authors:
- Kuo, Ting-Chun
Shaw, Jei-Fu
Lee, Guan-Chiun - Abstract:
- Graphical abstract: Highlights: Two combined processes were developed to improve Lip2 secretion in P. pastoris . The process includes gene copy amplification and low-temperature culture. The process results in a maximal 32-fold increase in Lip2 secretion. The steady-state LIP2 mRNA amount determines the maximal secretion level of Lip2. Abstract: The yeast Candida rugosa can secrete a mixture of lipase isoenzymes (Lips), which have been widely applied in industry. Eight Lip genes ( LIP1 to LIP8 ) have been identified and are expressed in Pichia pastoris . However, the expression level was not sufficient for economical industrial application. In this study, two combined processes of antibiotic selection and low-temperature culture efficiently elicited a high-level secretion of recombinant Lip2 in P. pastoris . The LIP2 gene copy number of the Pichia transformants was increased by sequential selections at gradually increasing Zeocin concentrations. After the first selection at 500 μg/mL of Zeocin, three clones (500-clones) with 2.4-fold to 5.8-fold improvement in Lip2 secretion were identified from 105 survival clones through lipase activity screening. Although the maximum number of LIP2 gene copy was four among these three 500-clones, the lipase secretion of the four-copy clone was not higher than that of the three-copy clone. The effects of multiple gene copy number and low culture temperature resulted in a maximal 32-fold increase in Lip2 secretion. This method could beGraphical abstract: Highlights: Two combined processes were developed to improve Lip2 secretion in P. pastoris . The process includes gene copy amplification and low-temperature culture. The process results in a maximal 32-fold increase in Lip2 secretion. The steady-state LIP2 mRNA amount determines the maximal secretion level of Lip2. Abstract: The yeast Candida rugosa can secrete a mixture of lipase isoenzymes (Lips), which have been widely applied in industry. Eight Lip genes ( LIP1 to LIP8 ) have been identified and are expressed in Pichia pastoris . However, the expression level was not sufficient for economical industrial application. In this study, two combined processes of antibiotic selection and low-temperature culture efficiently elicited a high-level secretion of recombinant Lip2 in P. pastoris . The LIP2 gene copy number of the Pichia transformants was increased by sequential selections at gradually increasing Zeocin concentrations. After the first selection at 500 μg/mL of Zeocin, three clones (500-clones) with 2.4-fold to 5.8-fold improvement in Lip2 secretion were identified from 105 survival clones through lipase activity screening. Although the maximum number of LIP2 gene copy was four among these three 500-clones, the lipase secretion of the four-copy clone was not higher than that of the three-copy clone. The effects of multiple gene copy number and low culture temperature resulted in a maximal 32-fold increase in Lip2 secretion. This method could be applied to other Lip isoforms to enhance their yields in P. pastoris . … (more)
- Is Part Of:
- Process biochemistry. Volume 50:Issue 12(2015:Dec.)
- Journal:
- Process biochemistry
- Issue:
- Volume 50:Issue 12(2015:Dec.)
- Issue Display:
- Volume 50, Issue 12 (2015)
- Year:
- 2015
- Volume:
- 50
- Issue:
- 12
- Issue Sort Value:
- 2015-0050-0012-0000
- Page Start:
- 2137
- Page End:
- 2143
- Publication Date:
- 2015-12
- Subjects:
- Lipase -- Multi-copy strains -- Temperature -- Secretion -- Pichia pastoris -- Candida rugosa
Biochemical engineering -- Periodicals
Biotechnology -- Periodicals
Biochemistry -- periodicals
Biotechnology -- periodicals
Chemical Engineering -- periodicals
Génie biochimique -- Périodiques
Biotechnologie -- Périodiques
Biochemical engineering
Biotechnology
Periodicals
660.63 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13595113 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.procbio.2015.09.013 ↗
- Languages:
- English
- ISSNs:
- 1359-5113
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6849.983500
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- 7788.xml