| Literature DB >> 25689311 |
Hideo Kawaguchi1, Hiroshi Teramura1, Kouji Uematsu1, Kiyotaka Y Hara2, Tomohisa Hasunuma2, Ko Hirano3, Takashi Sazuka3, Hidemi Kitano3, Yota Tsuge2, Prihardi Kahar1, Satoko Niimi-Nakamura1, Ken-Ichi Oinuma4, Naoki Takaya4, Shigemitsu Kasuga5, Chiaki Ogino1, Akihiko Kondo6.
Abstract
Dilute acid-pretreated sorghum bagasse, which was predominantly composed of glucan (59%) and xylose (7.2%), was used as a lignocellulosic feedstock for d-phenyllactic acid (PhLA) production by a recombinant Escherichia coli strain expressing phenylpyruvate reductase from Wickerhamia fluorescens. During fermentation with enzymatic hydrolysate of sorghum bagasse as a carbon source, the PhLA yield was reduced by 35% compared to filter paper hydrolysate, and metabolomics analysis revealed that NAD(P)H regeneration and intracellular levels of erythrose-4-phosphate and phosphoenolpyruvate for PhLA biosynthesis markedly reduced. Compared to separate hydrolysis and fermentation (SHF) with sorghum bagasse hydrolysate, simultaneous saccharification and fermentation (SSF) of sorghum bagasse under glucose limitation conditions yielded 4.8-fold more PhLA with less accumulation of eluted components, including p-coumaric acid and aldehydes, which inhibited PhLA fermentation. These results suggest that gradual enzymatic hydrolysis during SSF enhances PhLA production under glucose limitation and reduces the accumulation of fermentation inhibitors, collectively leading to increased PhLA yield.Entities:
Keywords: Fermentation inhibitor; Lignocellulosic biomass; Phenyllactic acid; Simultaneous saccharification and fermentation; Sorghum
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Year: 2015 PMID: 25689311 DOI: 10.1016/j.biortech.2015.01.097
Source DB: PubMed Journal: Bioresour Technol ISSN: 0960-8524 Impact factor: 9.642