2017
DOI: 10.1039/c7ra03176a
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Thermophilic Enterococcus faecium QU 50 enabled open repeated batch fermentation for l-lactic acid production from mixed sugars without carbon catabolite repression

Abstract: Thermophilic lactic acid bacterium enabled homo-l-lactic acid fermentation from hexose/pentose without carbon catabolite repression, and open repeated production by immobilization.

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Cited by 19 publications
(6 citation statements)
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“…The repeated batch process involves repeated cycles of fermentation by reinoculating a part or all of the cells from one batch fermentation broth into the next batch fermentation medium [30]. In comparison with batch or fed batch culture, repeated batch operation has proved to have several advantages in increasing LA productivity besides saving the time and labor work [30]. BoM1-2 strain was firstly cultivated in repeated batch fermentation using 60 g L −1 of glucose for 10 runs at controlled pH 9.0.…”
Section: Discussionmentioning
confidence: 99%
“…The repeated batch process involves repeated cycles of fermentation by reinoculating a part or all of the cells from one batch fermentation broth into the next batch fermentation medium [30]. In comparison with batch or fed batch culture, repeated batch operation has proved to have several advantages in increasing LA productivity besides saving the time and labor work [30]. BoM1-2 strain was firstly cultivated in repeated batch fermentation using 60 g L −1 of glucose for 10 runs at controlled pH 9.0.…”
Section: Discussionmentioning
confidence: 99%
“…The results showed that a L-LA productivity of 17.55 g•(L•h) −1 was obtained [59]. The immobilized strain QU 50 could produce stable L-LA with yield of 1.01-1.02 g•g −1 in an open repeated batch fermentation using mixed sugars derived from lignocellulosic biomass [60]. The mycelium of Rhizopus oryzae NBRC 5384 was fixed in situ in sponge-like cubic particles, and CaCO 3 was added to control the pH of the culture solution.…”
Section: High-cell Density Cultivationmentioning
confidence: 97%
“…CCR is the central governing mechanism in LAB for the regulation of rare sugar uptake, which ensures cellular resource efficiency by selectively regulating the uptake and metabolism of favorable carbon sources in the presence of non-favorable carbon sources, leading to both the favorable and non-favorable carbon sources can be metabolized albeit in a different rate [ 59 ]. In brief, CCR in LAB is regulated by different elements participating in rare sugar transport and metabolism, including sugar phosphotransferase system (PTS), enzyme I (EI), phosphocarrier histidine protein (HPr), and catabolite control protein A (CcpA) acts as the trans -acting repressor [ 60 ].…”
Section: Marine Macroalgae: the Future Of Sustainable Bioenergy And B...mentioning
confidence: 99%