| Literature DB >> 31639627 |
Deokyeol Jeong1, Suji Ye1, Heeyoung Park1, Soo Rin Kim2.
Abstract
Pectin-rich biomass has garnered attention as an alternative biomass source. However, some monomers derived from pectin-rich biomass, namely d-galacturonic acid, l-arabinose, and d-xylose, are not fermentable by industrial microorganisms such as Saccharomyces cerevisiae. The purpose of this study is to develop a S. cerevisiae strain capable of fermenting the pectin monomers. Expressions of eight heterologous genes and deletion of two endogenous genes, all of which were successfully completed by Cas9-based in vivo assembly and integration strategy, allowed the consumption of pectin monomers as sole carbon sources. To facilitate the consumption of galacturonic acid, which had the most limitations, the use of a co-substrate was tested using various sugars. As a result, we found that arabinose and xylose allowed simultaneous consumption of galacturonic acid. Based on intracellular metabolite profiling, it was concluded that the five-carbon sugars partially resolve the metabolic bottleneck of galacturonic acid.Entities:
Keywords: Bioethanol; CRISPR/Cas9; Citrus peel waste; Metabolic engineering; Pectin; Saccharomyces cerevisiae; Sugar beet pulp; d-galacturonic acid; l-arabinose
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Year: 2019 PMID: 31639627 DOI: 10.1016/j.biortech.2019.122259
Source DB: PubMed Journal: Bioresour Technol ISSN: 0960-8524 Impact factor: 9.642