Cargando…
Cofactor engineering improved CALB production in Pichia pastoris through heterologous expression of NADH oxidase and adenylate kinase
The cofactor engineering strategy can relieve the metabolic stress induced by expression of recombinant protein in cellular metabolism related to cofactor and energy reactions. To study the effect of cofactor regeneration on recombinant protein expression, NADH oxidase (noxE) was engineered in P. pa...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513558/ https://www.ncbi.nlm.nih.gov/pubmed/28715469 http://dx.doi.org/10.1371/journal.pone.0181370 |
_version_ | 1783250686920622080 |
---|---|
author | Jayachandran, Charumathi Palanisamy Athiyaman, Balakumaran Sankaranarayanan, Meenakshisundaram |
author_facet | Jayachandran, Charumathi Palanisamy Athiyaman, Balakumaran Sankaranarayanan, Meenakshisundaram |
author_sort | Jayachandran, Charumathi |
collection | PubMed |
description | The cofactor engineering strategy can relieve the metabolic stress induced by expression of recombinant protein in cellular metabolism related to cofactor and energy reactions. To study the effect of cofactor regeneration on recombinant protein expression, NADH oxidase (noxE) was engineered in P. pastoris expressing lipase B (GSCALB). Expression of noxE in P. pastoris (GSCALBNOX) increased NAD(+) levels by 85% with a concomitant reduction in NADH/NAD(+) ratio of 67% compared to GSCALB. The change in the redox level positively influenced the methanol uptake rate and made 34% augment in CALB activity. The decline in NADH level (44%) by noxE expression had lowered the adenylate energy charge (AEC) and ATP level in GSCALBNOX. In order to regenerate ATP in GSCALBNOX, adenylate kinase (ADK1) gene from S. cerevisiae S288c was co—expressed. Expression of ADK1 showed a remarkable increase in AEC and co—expression of both the genes synergistically improved CALB activity. This study shows the importance of maintenance of cellular redox homeostasis and adenylate energy charge during recombinant CALB expression in P. pastoris. |
format | Online Article Text |
id | pubmed-5513558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55135582017-08-07 Cofactor engineering improved CALB production in Pichia pastoris through heterologous expression of NADH oxidase and adenylate kinase Jayachandran, Charumathi Palanisamy Athiyaman, Balakumaran Sankaranarayanan, Meenakshisundaram PLoS One Research Article The cofactor engineering strategy can relieve the metabolic stress induced by expression of recombinant protein in cellular metabolism related to cofactor and energy reactions. To study the effect of cofactor regeneration on recombinant protein expression, NADH oxidase (noxE) was engineered in P. pastoris expressing lipase B (GSCALB). Expression of noxE in P. pastoris (GSCALBNOX) increased NAD(+) levels by 85% with a concomitant reduction in NADH/NAD(+) ratio of 67% compared to GSCALB. The change in the redox level positively influenced the methanol uptake rate and made 34% augment in CALB activity. The decline in NADH level (44%) by noxE expression had lowered the adenylate energy charge (AEC) and ATP level in GSCALBNOX. In order to regenerate ATP in GSCALBNOX, adenylate kinase (ADK1) gene from S. cerevisiae S288c was co—expressed. Expression of ADK1 showed a remarkable increase in AEC and co—expression of both the genes synergistically improved CALB activity. This study shows the importance of maintenance of cellular redox homeostasis and adenylate energy charge during recombinant CALB expression in P. pastoris. Public Library of Science 2017-07-17 /pmc/articles/PMC5513558/ /pubmed/28715469 http://dx.doi.org/10.1371/journal.pone.0181370 Text en © 2017 Jayachandran et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Jayachandran, Charumathi Palanisamy Athiyaman, Balakumaran Sankaranarayanan, Meenakshisundaram Cofactor engineering improved CALB production in Pichia pastoris through heterologous expression of NADH oxidase and adenylate kinase |
title | Cofactor engineering improved CALB production in Pichia pastoris through heterologous expression of NADH oxidase and adenylate kinase |
title_full | Cofactor engineering improved CALB production in Pichia pastoris through heterologous expression of NADH oxidase and adenylate kinase |
title_fullStr | Cofactor engineering improved CALB production in Pichia pastoris through heterologous expression of NADH oxidase and adenylate kinase |
title_full_unstemmed | Cofactor engineering improved CALB production in Pichia pastoris through heterologous expression of NADH oxidase and adenylate kinase |
title_short | Cofactor engineering improved CALB production in Pichia pastoris through heterologous expression of NADH oxidase and adenylate kinase |
title_sort | cofactor engineering improved calb production in pichia pastoris through heterologous expression of nadh oxidase and adenylate kinase |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5513558/ https://www.ncbi.nlm.nih.gov/pubmed/28715469 http://dx.doi.org/10.1371/journal.pone.0181370 |
work_keys_str_mv | AT jayachandrancharumathi cofactorengineeringimprovedcalbproductioninpichiapastoristhroughheterologousexpressionofnadhoxidaseandadenylatekinase AT palanisamyathiyamanbalakumaran cofactorengineeringimprovedcalbproductioninpichiapastoristhroughheterologousexpressionofnadhoxidaseandadenylatekinase AT sankaranarayananmeenakshisundaram cofactorengineeringimprovedcalbproductioninpichiapastoristhroughheterologousexpressionofnadhoxidaseandadenylatekinase |