Biosynthesis of geranate via isopentenol utilization pathway in Escherichia coli. Issue 1 (1st November 2022)

• Record Type: Journal Article
• Authors: Pan, Qiuchi; Ma, Xiaoqiang; Liang, Hong; Liu, Yurou; Zhou, Ying; Stephanopoulos, Gregory; Zhou, Kang
• Is Part Of: Biotechnology and bioengineering. Volume 120:Issue 1(2023)
• Page Start: 230
• Page End: 238
• Publication Date: 2022-11-01
• Subjects: geranate -- isopentenol utilization pathway -- isoprenoids -- metabolic engineering -- pathway engineering; Biotechnology -- Periodicals; Bioengineering -- Periodicals; 660.6
• DOI: 10.1002/bit.28255
• Languages: English
• ISSNs: 0006-3592

Abstract

Abstract: Isoprenoids are a large family of natural products with diverse structures, which allow them to play diverse and important roles in the physiology of plants and animals. They also have important commercial uses as pharmaceuticals, flavoring agents, fragrances, and nutritional supplements. Recently, metabolic engineering has been intensively investigated and emerged as the technology of choice for the production of isoprenoids through microbial fermentation. Isoprenoid biosynthesis typically originates in plants from acetyl‐coA in central carbon metabolism, however, a recent study reported an alternative pathway, the isopentenol utilization pathway (IUP), that can provide the building blocks of isoprenoid biosynthesis from affordable C5 substrates. In this study, we expressed the IUP in Escherichia coli to efficiently convert isopentenols into geranate, a valuable isoprenoid compound. We first established a geraniol‐producing strain in E. coli that uses the IUP. Then, we extended the geraniol synthesis pathway to produce geranate through two oxidation reactions catalyzed by two alcohol/aldehyde dehydrogenases from Castellaniella defragrans . The geranate titer was further increased by optimizing the expression of the two dehydrogenases and also parameters of the fermentation process. The best strain produced 764 mg/L geranate in 24 h from 2 g/L isopentenols (a mixture of isoprenol and prenol). We also investigated if the dehydrogenases could accept other isoprenoid alcohols as substrates.