食用菌学报
食用菌學報
식용균학보
ACTA EDULIS FUNGI
2009年
2期
67-71
,共5页
程俊文%吴学谦%贺亮%吴庆其%付立忠%魏海龙%李海波
程俊文%吳學謙%賀亮%吳慶其%付立忠%魏海龍%李海波
정준문%오학겸%하량%오경기%부립충%위해룡%리해파
香菇%子实体多糖%分步酶解%纤维素酶%果胶酶%木瓜蛋白酶
香菇%子實體多糖%分步酶解%纖維素酶%果膠酶%木瓜蛋白酶
향고%자실체다당%분보매해%섬유소매%과효매%목과단백매
Lentinula edodes%fruit body%polysaccharide extraction%stepwise enzymic hydrolysis%cellulose%pectinase%papain
首先采用正交试验优化纤维素酶﹑果胶酶和木瓜蛋白酶对香菇(Lentinula edodes)子实体多糖酶解提取的工艺参数,然后在优化酶解条件下,依次采用纤维素酶﹑果胶酶和木瓜蛋白酶分步处理香菇子实体以提取香菇多糖,并与单一酶解提取法和传统热水浸提法进行对比.结果表明,纤维素酶﹑果胶酶﹑木瓜蛋白酶的最佳提取工艺参数依次为加酶量0.8%、温度45 ℃、pH 4.5、提取时间1 h,加酶量1.0%、温度45 ℃、pH 3.5、提取时间2.0 h和加酶量1.0%、温度45 ℃、pH 4.0、提取时间1.5 h;在优化提取条件下,分步酶解法提取香菇粗多糖的提取率可达14.17%,比传统热水浸提法提高128.2%,比单独采用纤维素酶﹑果胶酶﹑木瓜蛋白酶酶解提取分别提高了43.71%、46.99%和23.11%.紫外光谱分析表明,分步酶解法提取的香菇多糖纯度明显高于热水浸提法提取的香菇多糖.-
首先採用正交試驗優化纖維素酶﹑果膠酶和木瓜蛋白酶對香菇(Lentinula edodes)子實體多糖酶解提取的工藝參數,然後在優化酶解條件下,依次採用纖維素酶﹑果膠酶和木瓜蛋白酶分步處理香菇子實體以提取香菇多糖,併與單一酶解提取法和傳統熱水浸提法進行對比.結果錶明,纖維素酶﹑果膠酶﹑木瓜蛋白酶的最佳提取工藝參數依次為加酶量0.8%、溫度45 ℃、pH 4.5、提取時間1 h,加酶量1.0%、溫度45 ℃、pH 3.5、提取時間2.0 h和加酶量1.0%、溫度45 ℃、pH 4.0、提取時間1.5 h;在優化提取條件下,分步酶解法提取香菇粗多糖的提取率可達14.17%,比傳統熱水浸提法提高128.2%,比單獨採用纖維素酶﹑果膠酶﹑木瓜蛋白酶酶解提取分彆提高瞭43.71%、46.99%和23.11%.紫外光譜分析錶明,分步酶解法提取的香菇多糖純度明顯高于熱水浸提法提取的香菇多糖.-
수선채용정교시험우화섬유소매﹑과효매화목과단백매대향고(Lentinula edodes)자실체다당매해제취적공예삼수,연후재우화매해조건하,의차채용섬유소매﹑과효매화목과단백매분보처리향고자실체이제취향고다당,병여단일매해제취법화전통열수침제법진행대비.결과표명,섬유소매﹑과효매﹑목과단백매적최가제취공예삼수의차위가매량0.8%、온도45 ℃、pH 4.5、제취시간1 h,가매량1.0%、온도45 ℃、pH 3.5、제취시간2.0 h화가매량1.0%、온도45 ℃、pH 4.0、제취시간1.5 h;재우화제취조건하,분보매해법제취향고조다당적제취솔가체14.17%,비전통열수침제법제고128.2%,비단독채용섬유소매﹑과효매﹑목과단백매매해제취분별제고료43.71%、46.99%화23.11%.자외광보분석표명,분보매해법제취적향고다당순도명현고우열수침제법제취적향고다당.-
The reaction conditions for enzymic extraction of polysaccharide from Lentinula edodes fruit bodies using cellulase, pectinase and papain individually were optimized using orthogonal testing L9(34). The respective optimal conditions for extraction with cellulase, pectinase and papain were as follows: (a) cellulose concentration 0.8%, temperature 45 ℃,pH 4.5,extraction time 1 h; (b) pectinase concentration 1.0%, temperature 45 ℃, pH 3.5,extraction time 2.0 h; (c) papain concentration 1.0%, temperature 45 ℃, pH 4.0,extraction time 1.5 h. Polysaccharide was then extracted using stepwise enzymic hydrolysis whereby each of the three enzymes was used successively under the respective optimal conditions. The traditional hot water extraction method was adopted as the control. The yield of polysaccharide extracted using stepwise enzymic hydrolysis (14.17%) was 128.2%, 43.71%, 46.99% and 23.11% higher, respectively compared with the individual yields obtained using hot water, cellulase, pectinase and papain. UV spectrophotometry revealed that the purity of the polysaccharide, as determined by Sevag's method, extracted using stepwise enzymic hydrolysis was higher compared to polysaccharide extracted using hot water.