The Taguchi method to find the solution to the fermentation of Ganoderma lucidum polysaccharides of soybean target process optimization study

碩士 === 國立勤益科技大學 === 研發科技與資訊管理研究所 === 98 === This paper adopts the concept of sensitivity analysis to find the range of the parameters that carries a greater impact to the processing parameters(Contains the air admission, PH, the temperature). The acquired result of the parameter range is referential...

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Main Authors: Liao Wen Pi, 廖文丕
Other Authors: Dr.Kuo-Liang Weng
Format: Others
Language:zh-TW
Published: 2010
Online Access:http://ndltd.ncl.edu.tw/handle/04977026933339453363
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spelling ndltd-TW-0983961052015-10-14T04:07:13Z http://ndltd.ncl.edu.tw/handle/04977026933339453363 The Taguchi method to find the solution to the fermentation of Ganoderma lucidum polysaccharides of soybean target process optimization study 運用田口法找出以靈芝大豆發酵液多醣體目標值最佳化製程之研究 Liao Wen Pi 廖文丕 碩士 國立勤益科技大學 研發科技與資訊管理研究所 98 This paper adopts the concept of sensitivity analysis to find the range of the parameters that carries a greater impact to the processing parameters(Contains the air admission, PH, the temperature). The acquired result of the parameter range is referential to Taguchi’s Method as the control factor level.Furthermore, Taguchi’s Method and variances are employed to analyze the level of contribution of respective control parameters towards the processing, so as to ask for a better control parameter combination for the most prolificacy of the polysaccharide target value. Its result to let Vaccination quantity 6%, amount of dissolved oxygen 90%, temperatures 30℃. Under the same fixed factor, before making the regulation improvement, the ganoderma lucidum polysaccharide body to deliver the quantity is 2.59-4.56 g/kg, but after improving, it delivers the quantity is 4.46-4.63 g/kg, therefore promotes according to this system Cheng Ke to produce the ganoderma lucidum polysaccharide body to deliver the quantity and to stabilize its yield rate. The first stage was by using soy-based (1.5% soybean protein isolate, 1.5 Brix molasses)medium for submerged culture of G. lucidium, by the β-glucosidasea of Ganoderma the biological inactive form soybean isoflavone will be transformation to more from the 16 to 5.5 double functional active aglycones, such as daidzein and genistein. The second stage was put Lactobacillus paracasei (LP) or Bifidobacter longum (BL) in Ganoderma lucidium to in the fermentation process. Also the exo-polysaccharids of Ganoderma has been use as a prebiotics to promote the growth of lactic acid bacteria up to 2 log CFU/mL. And the anti-oxygen DPPH’s IC50 evaluation was from 330.05 mg/mL up to LP bacterium’s 200.52 mg/mL and BL bacterium’s 178.27 mg/mL. This lactic acid fermentation stage could improve the flavor and to expand shelf-life of this novel lactate drink. Dr.Kuo-Liang Weng Dr.Shih-Chia Huang Dr.Wen-Tsann Lin 翁國亮博士 黃士嘉博士 林文燦博士 2010 學位論文 ; thesis 86 zh-TW
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language zh-TW
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description 碩士 === 國立勤益科技大學 === 研發科技與資訊管理研究所 === 98 === This paper adopts the concept of sensitivity analysis to find the range of the parameters that carries a greater impact to the processing parameters(Contains the air admission, PH, the temperature). The acquired result of the parameter range is referential to Taguchi’s Method as the control factor level.Furthermore, Taguchi’s Method and variances are employed to analyze the level of contribution of respective control parameters towards the processing, so as to ask for a better control parameter combination for the most prolificacy of the polysaccharide target value. Its result to let Vaccination quantity 6%, amount of dissolved oxygen 90%, temperatures 30℃. Under the same fixed factor, before making the regulation improvement, the ganoderma lucidum polysaccharide body to deliver the quantity is 2.59-4.56 g/kg, but after improving, it delivers the quantity is 4.46-4.63 g/kg, therefore promotes according to this system Cheng Ke to produce the ganoderma lucidum polysaccharide body to deliver the quantity and to stabilize its yield rate. The first stage was by using soy-based (1.5% soybean protein isolate, 1.5 Brix molasses)medium for submerged culture of G. lucidium, by the β-glucosidasea of Ganoderma the biological inactive form soybean isoflavone will be transformation to more from the 16 to 5.5 double functional active aglycones, such as daidzein and genistein. The second stage was put Lactobacillus paracasei (LP) or Bifidobacter longum (BL) in Ganoderma lucidium to in the fermentation process. Also the exo-polysaccharids of Ganoderma has been use as a prebiotics to promote the growth of lactic acid bacteria up to 2 log CFU/mL. And the anti-oxygen DPPH’s IC50 evaluation was from 330.05 mg/mL up to LP bacterium’s 200.52 mg/mL and BL bacterium’s 178.27 mg/mL. This lactic acid fermentation stage could improve the flavor and to expand shelf-life of this novel lactate drink.
author2 Dr.Kuo-Liang Weng
author_facet Dr.Kuo-Liang Weng
Liao Wen Pi
廖文丕
author Liao Wen Pi
廖文丕
spellingShingle Liao Wen Pi
廖文丕
The Taguchi method to find the solution to the fermentation of Ganoderma lucidum polysaccharides of soybean target process optimization study
author_sort Liao Wen Pi
title The Taguchi method to find the solution to the fermentation of Ganoderma lucidum polysaccharides of soybean target process optimization study
title_short The Taguchi method to find the solution to the fermentation of Ganoderma lucidum polysaccharides of soybean target process optimization study
title_full The Taguchi method to find the solution to the fermentation of Ganoderma lucidum polysaccharides of soybean target process optimization study
title_fullStr The Taguchi method to find the solution to the fermentation of Ganoderma lucidum polysaccharides of soybean target process optimization study
title_full_unstemmed The Taguchi method to find the solution to the fermentation of Ganoderma lucidum polysaccharides of soybean target process optimization study
title_sort taguchi method to find the solution to the fermentation of ganoderma lucidum polysaccharides of soybean target process optimization study
publishDate 2010
url http://ndltd.ncl.edu.tw/handle/04977026933339453363
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