Fermentation process for preparing xylitol using mutant cells
AssigneesTong Yang Confectionery Corp., Bolak Co., Ltd.
InventorsSang Yong Kim, Deok Kun Oh, Jin Hwan Choi, Soo Eun Kim
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Abstract
The present invention relates to a fermentation process for preparing xylitol with high productivity using novel mutant cells of Candida parapsilosis, more specifically, for preparing xylitol under optimal fermentation conditions for maximum xylitol production by optimizing the composition of medium containing xylose and the environmental conditions of culture such as pH, temperature and DO concentration, anal controlling the concentration of mutant cells.
Claims5
A fermentation process for maximum production of xylitol using mutant cells Candida parapsilosis deposited to Korean Culture Center of Microorganisms with accession number KCCM-10088 comprising the steps of:
- i) fermenting xylose medium with the mutant cells wherein
- a) the mutant cell concentration by centrifugation of mutant cells grown on xylose medium or by rapid accumulation of the cells during fermentation is 15.about.35 g/L;
- b) the medium consists of 5.about.12 (w/v) % of xylose, 0.2.about.2.0 (w/v) % of yeast extract, 0.2.about.2.0 (w/v) % of ammonium sulfate, 0.2.about.2.0 (w/v) % of KH.sub.2 PO.sub.4 and 0.01.about.0.2 (w/v) % of MgSO.sub.4.7H.sub.2 O;
- c) dissolved oxygen concentration in the medium is 0.1.about.5.0 (w/v) %;
- d) redox (reduction-oxidation) potential in the medium is 50.about.150 mV;
- e) pH of the fermentation medium is 4.5.about.5.5;
- and
- f) temperature of fermentation is 27.degree..about.33.degree. C.;
- ii) removing the mutant cells and other residue from the fermentation medium;
- and
- iii) separating and recovering xylitol from the fermentation medium of step (ii).
The novel mutant cells of Candida parapsilosis (KCCM-10088).
A method of isolating Candida parapsilosis mutants having the genotype of C. parapsilosis (KCCM-10088) comprising the steps of:
- i) spreading and culturing a wild type Candida parapsilosis (ATCC-21019) on yeast-malt extract (YM) medium containing 0.1% nitrosomethylguanidine (NTG);
- ii) isolating the produced colonies at least three times on YM medium;
- iii) spreading and culturing the colonies of step (ii) on YM medium under UV illumination of 250.about.270 nm;
- and
- iv) isolating the growing colonies.
Dependencies are inferred from the claim text.