| Literature DB >> 33659559 |
Tabinda Shakeel1,2, Zia Fatma1,2, Syed Shams Yazdani1,2.
Abstract
Microbial production of alkanes employing synthetic biology tools has gained tremendous attention owing to the high energy density and similarity of alkanes to existing petroleum fuels. One of the most commonly studied pathways includes the production of alkanes by AAR (acyl-ACP (acyl carrier protein) reductase)-ADO (aldehyde deformylating oxygenase) pathway. Here, the intermediates of fatty acid synthesis pathway are used as substrate by the AAR enzyme to make fatty aldehyde, which is then deformylated by ADO to make linear chain alkane. However, the variation in substrate availability to the first enzyme of the pathway, i.e., AAR, via fatty acid synthesis pathway and low turnover of the ADO enzyme make calculation of yields and titers under in vivo conditions extremely difficult. In vivo assay employing external addition of defined substrates for ADO enzyme into the medium helps to monitor the influx of substrate hence providing a more accurate measurement of the product yields. In this protocol, we include a detailed guide for implementing the in vivo assay for monitoring alkane production in E. coli.Entities:
Keywords: ADO; Alkanes; Biochemistry; Biofuels; Enzyme assay; Gas chromatography
Year: 2020 PMID: 33659559 PMCID: PMC7842645 DOI: 10.21769/BioProtoc.3593
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325