食品研究与开发
食品研究與開髮
식품연구여개발
FOOD RESEARCH AND CEVELOPMENT
2015年
14期
79-82
,共4页
李宏杰%方军%蒋彩霞%沈康
李宏傑%方軍%蔣綵霞%瀋康
리굉걸%방군%장채하%침강
γ-聚谷氨酸%枯草芽孢杆菌%发酵工艺
γ-聚穀氨痠%枯草芽孢桿菌%髮酵工藝
γ-취곡안산%고초아포간균%발효공예
γ-poly glutamic acid%Bacillus subtilis%fermentation process
采用发酵技术,利用枯草芽孢杆菌发酵生产γ-聚谷氨酸,对γ-聚谷氨酸发酵工艺进行研究.主要研究碳源、氮源、装液量、接种量、发酵时间、pH以及前体谷氨酸钠和促进剂氯化铵对γ-聚谷氨酸发酵的影响.前期研究表明,γ-聚谷氨酸发酵液黏度与其产量线性相关,故本研究中采用发酵液黏度作为γ-聚谷氨酸产量的衡量指标.通过单因素试验和正交试验,对发酵培养基和发酵条件进行优化,最后得到最佳发酵培养基配方和发酵条件.通过单因素及正交试验,确定最佳发酵培养基配方为:葡萄糖4%,酵母膏0.5%,谷氨酸钠3%,MgSO4·7H2O 0.025%,K2HPO4 0.2%,氯化铵0.3%;最佳发酵条件为:初始pH 9.5,装液量50mL,接种量6%,摇床转速为220 r/min,37℃振荡培养72 h.
採用髮酵技術,利用枯草芽孢桿菌髮酵生產γ-聚穀氨痠,對γ-聚穀氨痠髮酵工藝進行研究.主要研究碳源、氮源、裝液量、接種量、髮酵時間、pH以及前體穀氨痠鈉和促進劑氯化銨對γ-聚穀氨痠髮酵的影響.前期研究錶明,γ-聚穀氨痠髮酵液黏度與其產量線性相關,故本研究中採用髮酵液黏度作為γ-聚穀氨痠產量的衡量指標.通過單因素試驗和正交試驗,對髮酵培養基和髮酵條件進行優化,最後得到最佳髮酵培養基配方和髮酵條件.通過單因素及正交試驗,確定最佳髮酵培養基配方為:葡萄糖4%,酵母膏0.5%,穀氨痠鈉3%,MgSO4·7H2O 0.025%,K2HPO4 0.2%,氯化銨0.3%;最佳髮酵條件為:初始pH 9.5,裝液量50mL,接種量6%,搖床轉速為220 r/min,37℃振盪培養72 h.
채용발효기술,이용고초아포간균발효생산γ-취곡안산,대γ-취곡안산발효공예진행연구.주요연구탄원、담원、장액량、접충량、발효시간、pH이급전체곡안산납화촉진제록화안대γ-취곡안산발효적영향.전기연구표명,γ-취곡안산발효액점도여기산량선성상관,고본연구중채용발효액점도작위γ-취곡안산산량적형량지표.통과단인소시험화정교시험,대발효배양기화발효조건진행우화,최후득도최가발효배양기배방화발효조건.통과단인소급정교시험,학정최가발효배양기배방위:포도당4%,효모고0.5%,곡안산납3%,MgSO4·7H2O 0.025%,K2HPO4 0.2%,록화안0.3%;최가발효조건위:초시pH 9.5,장액량50mL,접충량6%,요상전속위220 r/min,37℃진탕배양72 h.
In this study, the fermentation technology was used to produce γ-PGA with Bacillus subtilis fermentation, and the fermentation process technology ofγ-PGA is studied. The influence of the output ofγ-PGA was the main researched, such as the carbon source, nitrogen source, liquid volume, inoculation , fermentation time, pH and sodium glutamate precursor and the promoter of ammonium chloride. Previous studies had shown thatγ-PGA fermentation broth viscosity linearly related to its production , the viscosity of the fermentation broth was used as γ-PGA output measure. The optimum medium composition and the optimum fermentation conditions scope were determined by single factor experiment orthogonal experiment. The optimum medium of the fermentation obtained through the single factor and orthogonal experiments was:4%glucose, 0.5%yeast extract, sodium glutamate 3%, MgSO4 7H2O 0.025%, K2HPO4 0.2%, ammonium chloride, 0.3%;Optimum fermentation conditions were: initial pH 9.5, medium volume 50mL, inoculum size 6 %, rotation speed of 220 r/min, 37℃oscillator cultured 72 h.