| Literature DB >> 33968571 |
Dharam Pal1, Gopal Patel2,3, Prakashkumar Dobariya1, Shivraj Hariram Nile3, Abhay H Pande1, Uttam Chand Banerjee2.
Abstract
Recombinant human interferon-β (rhIFN-β) is therapeutically important and new commercially viable approaches are needed for its increased production. In this study, a codon-optimized gene encoding for rhIFN-β(C17S) protein was designed and expressed in E. coli SE1. As a first step of medium optimization, growth of E. coli as a function of different media components was studied. Subsequently, to optimize the media composition, a response surface methodology (RSM) was used. Our results show that optimized medium (15.0 g/L tryptone, 12.3 g/L meat extract, 1.0 g/L MgSO4 and 0.5 g/L thiamine along with minimal medium) obtained in this study provide better growth of recombinant cells and the expression level of recombinant protein was ~ 1.7-fold more than Luria-Bertani medium. The optimized medium may be utilized for the large-scale production of rhIFN-β. © King Abdulaziz City for Science and Technology 2021.Entities:
Keywords: Central composite design; Luria–Bertani medium; Plackett–Burman design; Recombinant human interferon-beta; Response surface methodology
Year: 2021 PMID: 33968571 PMCID: PMC8055739 DOI: 10.1007/s13205-021-02772-1
Source DB: PubMed Journal: 3 Biotech ISSN: 2190-5738 Impact factor: 2.406