Production and release of chitinase by recombinant Escherichia coli.
碩士 === 國立成功大學 === 化學工程研究所 === 83 === The factors that improve recombinant protein excretion efficiency were investigated. The factors discussed in this dissertation include the ratio of carbon to nitrogen source (C/ N ratio), the addition o...
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ndltd-TW-083NCKU00630442015-10-13T12:53:32Z http://ndltd.ncl.edu.tw/handle/95842215056398661626 Production and release of chitinase by recombinant Escherichia coli. 分泌性基因重組幾丁分解酵素在大腸桿菌表現與釋放至菌體外之研究 Ming-Ching Huang 黃明清 碩士 國立成功大學 化學工程研究所 83 The factors that improve recombinant protein excretion efficiency were investigated. The factors discussed in this dissertation include the ratio of carbon to nitrogen source (C/ N ratio), the addition of glycine and EDTA, the addition of alkali metal ions, and the supplement of guanidine-HCl. First, the result was shown that the excretion of model protein- chitinase was more obvious in the C/N ratio=0.1 than the other following C/N ratios. Second, it was indicated that the excretion ofchitinase increased with glycine and EDTA concentration. Besides, addition time of glycine and EDTA also influences the release of protein. Next, it was found that supplement of alkali metal ions would improve chitinase produ- ction and excretion, especially Na+. Although addition of guan- idine-HCl in growing cell culture broth, protein was denatured besides cell growth limited. It was thought that the improve- ment of chitinaseexcretion into culture medium by the factors mentioned abovewere primary due to cell outer membrane perme- ability. Professor Chu-Yuan Cheng 鄭智元 1995 學位論文 ; thesis 55 zh-TW |
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zh-TW |
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碩士 === 國立成功大學 === 化學工程研究所 === 83 === The factors that improve recombinant protein excretion
efficiency were investigated. The factors discussed in this
dissertation include the ratio of carbon to nitrogen source (C/
N ratio), the addition of glycine and EDTA, the addition of
alkali metal ions, and the supplement of guanidine-HCl. First,
the result was shown that the excretion of model protein-
chitinase was more obvious in the C/N ratio=0.1 than the other
following C/N ratios. Second, it was indicated that the
excretion ofchitinase increased with glycine and EDTA
concentration. Besides, addition time of glycine and EDTA also
influences the release of protein. Next, it was found that
supplement of alkali metal ions would improve chitinase produ-
ction and excretion, especially Na+. Although addition of guan-
idine-HCl in growing cell culture broth, protein was denatured
besides cell growth limited. It was thought that the improve-
ment of chitinaseexcretion into culture medium by the factors
mentioned abovewere primary due to cell outer membrane perme-
ability.
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author2 |
Professor Chu-Yuan Cheng |
author_facet |
Professor Chu-Yuan Cheng Ming-Ching Huang 黃明清 |
author |
Ming-Ching Huang 黃明清 |
spellingShingle |
Ming-Ching Huang 黃明清 Production and release of chitinase by recombinant Escherichia coli. |
author_sort |
Ming-Ching Huang |
title |
Production and release of chitinase by recombinant Escherichia coli. |
title_short |
Production and release of chitinase by recombinant Escherichia coli. |
title_full |
Production and release of chitinase by recombinant Escherichia coli. |
title_fullStr |
Production and release of chitinase by recombinant Escherichia coli. |
title_full_unstemmed |
Production and release of chitinase by recombinant Escherichia coli. |
title_sort |
production and release of chitinase by recombinant escherichia coli. |
publishDate |
1995 |
url |
http://ndltd.ncl.edu.tw/handle/95842215056398661626 |
work_keys_str_mv |
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