Please use this identifier to cite or link to this item: http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/1094
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dc.contributor.authorInparuban, K.-
dc.contributor.authorBalakumar, S.-
dc.contributor.authorVasantharuba, S.-
dc.contributor.authorArasaratnam, V.-
dc.date.accessioned2018-01-25T06:29:42Z-
dc.date.accessioned2022-06-24T07:39:03Z-
dc.date.available2018-01-25T06:29:42Z-
dc.date.available2022-06-24T07:39:03Z-
dc.date.issued2009-
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/1094-
dc.description.abstractThe aim of this study was to find out suitable culture conditions to improve the cell mass production of Saccharomyces cerevisiae. S.cerevisiae was grown in a medium(300C, pH 5.0) with sucrose (Table sugar) from 10 to 50 g/L-1 along with (g/L-1) yeast extract (2.5), bacteriological peptone(1.15), NH4HPO4(0.25) and MgSO4.7H2O(0.025). Highest cell mass of 4.43 g/L-1 was obtained in the medium with 50 g/L-1 of sucrose. When the oxygen supply and diffusion were improved by either, mixing in a shaker (100rpm), by an impellor (100 rpm) or aeration (100 bubbles/min), highest cell mass (4.52 g/L-1) was obtained with aeration. Increase in aeration rate to 200bubbles/min increased the yeast cell mass to 5.41 g/L-1. For volumetric scaling up, medium to flask volume ratio was maintained as 1:2, in 1,2,3 and 5 L flasks, and the highest cell mass (5.53 g/L-1) was produced in 2L flask. By optimizing the culture conditions the yeast cell mass production was increased by 1.25 timesen_US
dc.language.isoen_USen_US
dc.subjectBaker’s yeasten_US
dc.subjectCell mass productionen_US
dc.subjectAerationen_US
dc.subjectReaction volume ratioen_US
dc.titleOPTIMIZATION OF CULTURE CONDITIONS FOR BAKER’S YEAST CELL MASS PRODUCTION- A PRELIMINARY STUDYen_US
dc.typeArticleen_US
Appears in Collections:Agricultural Chemistry

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