福建师范大学学报(自然科学版)
福建師範大學學報(自然科學版)
복건사범대학학보(자연과학판)
JOURNAL OF FUJIAN TEACHERS UNIVERSITY(NATURAL SCIENCE)
2010年
1期
103-108
,共6页
黄维雅%刘艳如%蓝灿华%黄建忠
黃維雅%劉豔如%藍燦華%黃建忠
황유아%류염여%람찬화%황건충
正红菇%菌丝体%凝集素%响应面法%优化
正紅菇%菌絲體%凝集素%響應麵法%優化
정홍고%균사체%응집소%향응면법%우화
Russula vinosa%mycelium%lectin%response surface methodology%optimization
采用响应面法对液体深层培养的正红菇(Russula vinosa)菌丝体产胞内凝集素的培养条件进行了优化.通过单因子实验确定最适碳源和氮源为淀粉和酵母膏,在此基础上,通过Plackett-Burrman设计对影响其产胞内凝集素的相关因素进行评估并筛选出具有显著效应的淀粉、酵母膏、装液量3个因素,通过最陡爬坡实验及响应面分析法确定了产凝集素的最适条件:ω(淀粉)3.04%,ω(酵母膏)0.3%,ω(KH_2PO_4)0.2%,ω(MgSO_4)0.1%,装液量73 mL,转速250 r/min,初始pH 5,发酵时间5 d.在此条件下,菌丝体产胞内凝集素的总活力可达72 127.3 u,与初始培养条件下的凝集素总活力相比提高了1.88倍.
採用響應麵法對液體深層培養的正紅菇(Russula vinosa)菌絲體產胞內凝集素的培養條件進行瞭優化.通過單因子實驗確定最適碳源和氮源為澱粉和酵母膏,在此基礎上,通過Plackett-Burrman設計對影響其產胞內凝集素的相關因素進行評估併篩選齣具有顯著效應的澱粉、酵母膏、裝液量3箇因素,通過最陡爬坡實驗及響應麵分析法確定瞭產凝集素的最適條件:ω(澱粉)3.04%,ω(酵母膏)0.3%,ω(KH_2PO_4)0.2%,ω(MgSO_4)0.1%,裝液量73 mL,轉速250 r/min,初始pH 5,髮酵時間5 d.在此條件下,菌絲體產胞內凝集素的總活力可達72 127.3 u,與初始培養條件下的凝集素總活力相比提高瞭1.88倍.
채용향응면법대액체심층배양적정홍고(Russula vinosa)균사체산포내응집소적배양조건진행료우화.통과단인자실험학정최괄탄원화담원위정분화효모고,재차기출상,통과Plackett-Burrman설계대영향기산포내응집소적상관인소진행평고병사선출구유현저효응적정분、효모고、장액량3개인소,통과최두파파실험급향응면분석법학정료산응집소적최괄조건:ω(정분)3.04%,ω(효모고)0.3%,ω(KH_2PO_4)0.2%,ω(MgSO_4)0.1%,장액량73 mL,전속250 r/min,초시pH 5,발효시간5 d.재차조건하,균사체산포내응집소적총활력가체72 127.3 u,여초시배양조건하적응집소총활력상비제고료1.88배.
Russula vinosa fermentation recipe was optimized by surface response methodology to improve production of lectin from mycelium of Russula vinosa. The optimum carbon and nitrogen for Russula vinosa mycelium were obtained through monofactorial experiment, which were starch and yeast extract respectively. Through Plackett-Burrman design some process factors of intracellular lectin production were evaluated and three factors had prominent effect on intracellular lectin production were picked out, which were starch, yeast extract and liquid volume respectively. The steepest ascent search and response surface analysis were used to estimate optimum culture condition. It was composed of 3.04% starch, 0.3% yeast extract, 0.2% KH_2PO_4, 0.1% MgSO_4,liquid volume 73 mL,250 r/min,pH 5,fermentation time 5 d. As a result , the total agglutinating activity of intracellular lectin was increased to 72 127.3 u, which was improved 1.88-fold compared to the original conditions.