2020
DOI: 10.1021/acsomega.0c02089
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Comparative Glucose and Xylose Coutilization Efficiencies of Soil-Isolated Yeast Strains Identify Cutaneotrichosporon dermatis as a Potential Producer of Lipid

Abstract: Glucose and xylose are the major hydrolysates of lignocellulose, and therefore, it is of great implication to identify the microbes involved in simultaneous utilization of glucose and xylose. In this study, the strain ZZ-46 isolated from the soil of Nanyang, China, could simultaneously assimilate glucose and xylose efficiently to produce lipid. Upon cultivation with a 2:1 glucose/xylose mixture as the carbon source for 144 h, the cell biomass, lipid concentration, lipid content, and lipid yield of ZZ-46 reache… Show more

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Cited by 10 publications
(6 citation statements)
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“…Yet, the modified strains created by these techniques are incapable of efficiently co-utilizing xylose and glucose. The strain C. dermatis NICC30027 demonstrated natural capacity to consume xylose and glucose [ 15 ]. In our opinion, one of the following conditions exists in the strain C. dermatis NICC30027: i) there is a high level of the cAMP-CAP complex in the cell due to some unknown metabolic mechanisms; ii) the expressions of key genes involved in xylose metabolism do not require cAMP-CAP mediated activation.…”
Section: Discussionmentioning
confidence: 99%
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“…Yet, the modified strains created by these techniques are incapable of efficiently co-utilizing xylose and glucose. The strain C. dermatis NICC30027 demonstrated natural capacity to consume xylose and glucose [ 15 ]. In our opinion, one of the following conditions exists in the strain C. dermatis NICC30027: i) there is a high level of the cAMP-CAP complex in the cell due to some unknown metabolic mechanisms; ii) the expressions of key genes involved in xylose metabolism do not require cAMP-CAP mediated activation.…”
Section: Discussionmentioning
confidence: 99%
“…The NICC30027 strain was cultured in YPD medium (glucose 20 g/L, yeast extract 10 g/L, and peptone 10 g/L) at 30°C with constant shaking (180 rpm) [ 15 ]. Cultures were established by inoculating a single colony in 10 mL of YPD medium in a 50 mL flask and culturing the cells overnight, followed by the transfer of 1 mL of this solution to 100 mL of YPD medium in a 500 mL flask.…”
Section: Methodsmentioning
confidence: 99%
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