2020
DOI: 10.1002/fsn3.1792
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Production, medium optimization, and structural characterization of an extracellular polysaccharide produced byRhodotorula minuta ATCC 10658

Abstract: Several strains of microorganism are capable of converting carbohydrates into extracellular polysaccharide. The preset research is a first effort made to optimize extracellular polysaccharide (CRMEP) by Rhodotorula minuta ATCC 10658 using one factor at time and response surface methods. One factor at time was applied in the initial screening of substrates prior to optimization study. Of all the substrates examined, starch as carbon source and defatted soy bean powder as protein source were discovered to be bes… Show more

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Cited by 6 publications
(4 citation statements)
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References 35 publications
(38 reference statements)
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“…Exopolysaccharide from Rhodotorula mucilaginosa CICC 33013 was composed of galactose, arabinose, glucose, and mannose ( 11 ). EPS of R. minuta ATCC 10658 consisted of mannose and glucose at a molar ratio of about 1.4:7.7 ( 29 ). The compositions of exopolysaccharides from a new cold-adapted R. mucilaginosa sp.…”
Section: Resultsmentioning
confidence: 99%
“…Exopolysaccharide from Rhodotorula mucilaginosa CICC 33013 was composed of galactose, arabinose, glucose, and mannose ( 11 ). EPS of R. minuta ATCC 10658 consisted of mannose and glucose at a molar ratio of about 1.4:7.7 ( 29 ). The compositions of exopolysaccharides from a new cold-adapted R. mucilaginosa sp.…”
Section: Resultsmentioning
confidence: 99%
“…Carbon sources are important factors determining the amount and the physicochemical characteristics of bacterial EPS [44]. Starch was ranked as the best substrate for extracellular polysaccharide production from Rhodotorula minuta ATCC 10,658 [65], as well as for Streptomyces sp. MOE6 in this work.…”
Section: Discussionmentioning
confidence: 99%
“…The solution was deproteinated by sevag method (1-butanol: chloroform at a ratio of 1:4, v/v; Staub, 1965 ). The sevag reagent was removed and a vacuum rotary evaporator (Heidolph Laborota, Germany) was employed to remove 2/3 water phase (supernatant), and then dialyzed against deionized water for 48 h. The concentrated water-soluble polysaccharides were precipitated by using 96% ethanol maintained at 4°C for 24 h. The precipitated polysaccharides were collected by centrifugation, and a vacuum Alpha 1–2 freeze-dryer (Christ, Germany) was used to attain crude G. lucidum polysaccharides (CGLP; Samadlouie et al, 2020 ).…”
Section: Methodsmentioning
confidence: 99%