Product Analysis and Mass Production Process Development of Green Tea Beverage Fermented by Saccharomyces cerevisiae

碩士 === 高苑科技大學 === 化工與生化工程研究所 === 100 === It is new emerging style for tea drink preparation by applying food microbiological fermentation differed in traditional tea manufacture. In previous study, we have successfully produced the low- or high-ethanol ethanol drink by yeast, Saccharomyces cerevisia...

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Main Authors: Chen Yan Chang, 陳彥彰
Other Authors: 王盛世
Format: Others
Language:zh-TW
Published: 2011
Online Access:http://ndltd.ncl.edu.tw/handle/07789628298226465347
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spelling ndltd-TW-100KYIT05660042015-10-13T20:52:03Z http://ndltd.ncl.edu.tw/handle/07789628298226465347 Product Analysis and Mass Production Process Development of Green Tea Beverage Fermented by Saccharomyces cerevisiae 以酵母菌製備綠茶飲料之量產製程開發與分析 Chen Yan Chang 陳彥彰 碩士 高苑科技大學 化工與生化工程研究所 100 It is new emerging style for tea drink preparation by applying food microbiological fermentation differed in traditional tea manufacture. In previous study, we have successfully produced the low- or high-ethanol ethanol drink by yeast, Saccharomyces cerevisias Meyen ex Haxen , fermenting green tea liquid which were composed of 25 g green tea, 750 mL RO water, and various amount of sucrose. In order to expand its production capacity in this study, the fermentation were performed at room temperature by mixing 300 g green tea with 2%, 8% or 16% sucrose and yeast in 3000 mL RO water. The fermented green tea liquids were sampled to analyze the yeast growth and the change of tea contents during the fermented period. The yeasts are the major dominant species in 2%、8% and 16% green-tea fermented liquid solutions. As a whole, the yeast growth has demonstrated to be an increasing growth tendency which first repetitively increased and then decreased, and trended again, etc. All the fermented green tea liquids contained obvious amount of total polyphenolics that is between 0.055 and 0.115 mg gallic acid equivalents/ml. All the fermented green tea liquids contained potent antioxidant activity. The DPPH radical scavenging activity is between 0.055 and 0.095 mg Trolox equivalents/ml. Although there were sucrose-added difference at the beginning fermentation stage, the difference of total sugar amount among all tested groups became less obvious after later stage’s fermentation.。By GC analysis, more ethanol production occurred at higher sucrose-added groups. The 16% green-tea fermented liquid has the highest ethanol production. All 2%, 8% and 16% green-tea fermented liquid can not be detected the existence of methanol, but little acetic acid. By HPLC analysis, all fermented green tea liquids have demonstrated obvious tea polyphenols amount and distribution. Therefore, all sucrose-added groups can produce safe tea drink. Based on aforementioned information, the fermented green tea liquid has potentially become an excellent health-protection drink. 王盛世 2011 學位論文 ; thesis 30 zh-TW
collection NDLTD
language zh-TW
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description 碩士 === 高苑科技大學 === 化工與生化工程研究所 === 100 === It is new emerging style for tea drink preparation by applying food microbiological fermentation differed in traditional tea manufacture. In previous study, we have successfully produced the low- or high-ethanol ethanol drink by yeast, Saccharomyces cerevisias Meyen ex Haxen , fermenting green tea liquid which were composed of 25 g green tea, 750 mL RO water, and various amount of sucrose. In order to expand its production capacity in this study, the fermentation were performed at room temperature by mixing 300 g green tea with 2%, 8% or 16% sucrose and yeast in 3000 mL RO water. The fermented green tea liquids were sampled to analyze the yeast growth and the change of tea contents during the fermented period. The yeasts are the major dominant species in 2%、8% and 16% green-tea fermented liquid solutions. As a whole, the yeast growth has demonstrated to be an increasing growth tendency which first repetitively increased and then decreased, and trended again, etc. All the fermented green tea liquids contained obvious amount of total polyphenolics that is between 0.055 and 0.115 mg gallic acid equivalents/ml. All the fermented green tea liquids contained potent antioxidant activity. The DPPH radical scavenging activity is between 0.055 and 0.095 mg Trolox equivalents/ml. Although there were sucrose-added difference at the beginning fermentation stage, the difference of total sugar amount among all tested groups became less obvious after later stage’s fermentation.。By GC analysis, more ethanol production occurred at higher sucrose-added groups. The 16% green-tea fermented liquid has the highest ethanol production. All 2%, 8% and 16% green-tea fermented liquid can not be detected the existence of methanol, but little acetic acid. By HPLC analysis, all fermented green tea liquids have demonstrated obvious tea polyphenols amount and distribution. Therefore, all sucrose-added groups can produce safe tea drink. Based on aforementioned information, the fermented green tea liquid has potentially become an excellent health-protection drink.
author2 王盛世
author_facet 王盛世
Chen Yan Chang
陳彥彰
author Chen Yan Chang
陳彥彰
spellingShingle Chen Yan Chang
陳彥彰
Product Analysis and Mass Production Process Development of Green Tea Beverage Fermented by Saccharomyces cerevisiae
author_sort Chen Yan Chang
title Product Analysis and Mass Production Process Development of Green Tea Beverage Fermented by Saccharomyces cerevisiae
title_short Product Analysis and Mass Production Process Development of Green Tea Beverage Fermented by Saccharomyces cerevisiae
title_full Product Analysis and Mass Production Process Development of Green Tea Beverage Fermented by Saccharomyces cerevisiae
title_fullStr Product Analysis and Mass Production Process Development of Green Tea Beverage Fermented by Saccharomyces cerevisiae
title_full_unstemmed Product Analysis and Mass Production Process Development of Green Tea Beverage Fermented by Saccharomyces cerevisiae
title_sort product analysis and mass production process development of green tea beverage fermented by saccharomyces cerevisiae
publishDate 2011
url http://ndltd.ncl.edu.tw/handle/07789628298226465347
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