Study on the production of chitosanase and bioactive materials from squid pen fermentation by Bacillus sp. TKU004

碩士 === 淡江大學 === 生命科學研究所碩士班 === 97 === This study focused on the utilization of squid pen as the sole carbon/nitrogen source by Bacillus sp. TKU004 to produce chitosanase and bioactive materials. The optimized culture condition for chitosanase production was composed of 3% squid pen powder (SPP),...

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Main Authors: Pei-Chen Wu, 吳倍甄
Other Authors: 王三郎
Format: Others
Language:zh-TW
Published: 2009
Online Access:http://ndltd.ncl.edu.tw/handle/72631750065459761043
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spelling ndltd-TW-097TKU051050022015-10-13T16:13:31Z http://ndltd.ncl.edu.tw/handle/72631750065459761043 Study on the production of chitosanase and bioactive materials from squid pen fermentation by Bacillus sp. TKU004 Bacillussp.TKU004發酵烏賊軟骨所生產幾丁聚醣酶及生物活性物質之研究 Pei-Chen Wu 吳倍甄 碩士 淡江大學 生命科學研究所碩士班 97 This study focused on the utilization of squid pen as the sole carbon/nitrogen source by Bacillus sp. TKU004 to produce chitosanase and bioactive materials. The optimized culture condition for chitosanase production was composed of 3% squid pen powder (SPP), 0.1% K2HPO4, 0.05% MgSO4.7H2O (pH 7), with autoclave treatment for 45 min, afterward, TKU004 was incubated in 100 mL of above liquid medium in an Erlenmeyer flask (250 mL) and kept shaking at 30℃ for two days. The chitosanase was purified from the culture supernatant by using ammonium sulfate precipitation, chromatography procedures of DEAE-Sepharose, Macro-Prep DEAE, and Sephacryl S-100. The overall activity yield of the purified chitosanase was 20%, with specific chitosanase activity of 2.8 U/mg. The molecular mass of TKU004 chitosanase determined by SDS-PAGE and gel filtration was approximately 29 kDa and 25 kDa, respectively. The results of peptide mass mapping indicated that TKU004 chitosanase matched to chitosanase from B. subtilis subsp. subtilis str. 168 (GenBank accession number gi16079742) with 23% sequence coverage. The optimum temperature, optimum pH, thermal stability, and pH stability of TKU004 chitosanase were 37℃, pH 7, <40℃, and pH 4~7, respectively. The chitosanase was inhibited by 5 mM Cu2+ and Fe2+, but retained 94%, 96%, 93%, 95% of its original activity in the presence of 2% Tween 20, 2% Tween 40, 2% Triton X-100, and 2 mM SDS, respectively. Additionally, TKU004 was cultivated for 1~6 days by using squid pen powder and shrimp head powder as the different carbon/nitrogen sources. The results indicated that culture supernatant (3% SPP) had higher DPPH free radical scavenging effect at the third day and better total phenolic contents, reducing activity, and Fe2+ chelating ability at the fifth day. 王三郎 2009 學位論文 ; thesis 76 zh-TW
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language zh-TW
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description 碩士 === 淡江大學 === 生命科學研究所碩士班 === 97 === This study focused on the utilization of squid pen as the sole carbon/nitrogen source by Bacillus sp. TKU004 to produce chitosanase and bioactive materials. The optimized culture condition for chitosanase production was composed of 3% squid pen powder (SPP), 0.1% K2HPO4, 0.05% MgSO4.7H2O (pH 7), with autoclave treatment for 45 min, afterward, TKU004 was incubated in 100 mL of above liquid medium in an Erlenmeyer flask (250 mL) and kept shaking at 30℃ for two days. The chitosanase was purified from the culture supernatant by using ammonium sulfate precipitation, chromatography procedures of DEAE-Sepharose, Macro-Prep DEAE, and Sephacryl S-100. The overall activity yield of the purified chitosanase was 20%, with specific chitosanase activity of 2.8 U/mg. The molecular mass of TKU004 chitosanase determined by SDS-PAGE and gel filtration was approximately 29 kDa and 25 kDa, respectively. The results of peptide mass mapping indicated that TKU004 chitosanase matched to chitosanase from B. subtilis subsp. subtilis str. 168 (GenBank accession number gi16079742) with 23% sequence coverage. The optimum temperature, optimum pH, thermal stability, and pH stability of TKU004 chitosanase were 37℃, pH 7, <40℃, and pH 4~7, respectively. The chitosanase was inhibited by 5 mM Cu2+ and Fe2+, but retained 94%, 96%, 93%, 95% of its original activity in the presence of 2% Tween 20, 2% Tween 40, 2% Triton X-100, and 2 mM SDS, respectively. Additionally, TKU004 was cultivated for 1~6 days by using squid pen powder and shrimp head powder as the different carbon/nitrogen sources. The results indicated that culture supernatant (3% SPP) had higher DPPH free radical scavenging effect at the third day and better total phenolic contents, reducing activity, and Fe2+ chelating ability at the fifth day.
author2 王三郎
author_facet 王三郎
Pei-Chen Wu
吳倍甄
author Pei-Chen Wu
吳倍甄
spellingShingle Pei-Chen Wu
吳倍甄
Study on the production of chitosanase and bioactive materials from squid pen fermentation by Bacillus sp. TKU004
author_sort Pei-Chen Wu
title Study on the production of chitosanase and bioactive materials from squid pen fermentation by Bacillus sp. TKU004
title_short Study on the production of chitosanase and bioactive materials from squid pen fermentation by Bacillus sp. TKU004
title_full Study on the production of chitosanase and bioactive materials from squid pen fermentation by Bacillus sp. TKU004
title_fullStr Study on the production of chitosanase and bioactive materials from squid pen fermentation by Bacillus sp. TKU004
title_full_unstemmed Study on the production of chitosanase and bioactive materials from squid pen fermentation by Bacillus sp. TKU004
title_sort study on the production of chitosanase and bioactive materials from squid pen fermentation by bacillus sp. tku004
publishDate 2009
url http://ndltd.ncl.edu.tw/handle/72631750065459761043
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