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枯草芽孢杆菌产β-甘露聚糖酶的发酵条件优化分析(英文)

Optimization of β-mannase production by bacillus subtilis
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摘要 为获得枯草芽孢杆菌产β-甘露聚糖酶的最佳发酵条件,分别对碳源、氮源、碳氮质量比、发酵时间和培养温度进行了单因素实验,在此基础上对发酵温度、接种量、培养基初始pH值和发酵时间四因素进行了L9(34)正交优化试验.结果表明枯草芽孢杆菌分泌β-甘露聚糖酶的最佳碳源为40 g/L魔芋精粉,最佳氮源为5 g/L酵母抽提物,两者最佳质量比为5∶1,最佳发酵条件为30℃的条件下摇瓶培养28 h;最佳发酵参数组合为发酵温度30℃、接种量5%、培养基初始pH6.5、发酵时间28 h;各因素对枯草芽孢杆菌产β-甘露聚糖酶的影响程度大小依次为发酵时间>发酵温度>接种量>培养基初始pH,其中发酵时间对产酶的影响最为显著. Mono-factor and orthogonal analysis were applicd to obtain the optimal fermentation conditions for β- mannase from Bacillus subtilis. The five factors: carbon, nitrogen, ratio of carbon and nitrogen, incubating temperature and incubation time were tested respectively. The four factors,including incubating temperature, inoculum size, original pH value and incubation time were designed in L9(3^4 ) for orthogonal analysis on the basis of mono-factor analysis. The result showed the optimal carbon, nitrogen, their optimal mass concentrations and their mass ratio are kanjac powder, yeast extract, 40 g/L, 5 g/L and 5 : 1 respectively. The optimal incubation temperature is 30 ℃, by 28 h. The optimal parameter group was incubating temperature 30 ℃, inoculum size 5 %, original pH 6.5 and incubation time 28 h. Effect on β-mannase activity drops according to the order of incubation time, incubating temperature, inoculum size and pH. Incubation time has a remarkable effect on production of β-mannasc.
出处 《安徽工程科技学院学报(自然科学版)》 2008年第1期1-6,共6页 Journal of Anhui University of Technology and Science
基金 a grant from Anhui academy youth sponsored project(2005jql071) Anhui academy sponsored project in natural science(kj2007b114)
关键词 枯草芽孢杆菌 Β-甘露聚糖酶 正交分析 Bacillus subtilis β-mannase Orthogonal analysis
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  • 1熊郃,干信.β-甘露聚糖酶产生菌R_(10)发酵条件研究[J].湖北工学院学报,2004,19(1):17-19. 被引量:7
  • 2杨文博,沈庆,佟树敏.产β-甘露聚糖酶地衣芽孢杆菌的分离筛选及发酵条件[J].微生物学通报,1995,22(3):154-157. 被引量:42
  • 3杨文博,佟树敏,沈庆,陈允,陈锦英.β-甘露聚糖酶酶解植物胶及其产物对双歧杆菌的促生长作用[J].微生物学通报,1995,22(4):204-207. 被引量:59
  • 4Charrier M, Rouland C. Mannan-degrading enzymes purified from the brown garden snail Helic aspersa Muller[J]. Journal of Experimental Zoology, 2001,290:125-135.
  • 5Takahashi R, Mizumoto K, Takano T, et al. Production of oligosaeeharides from hemieellulose of woody biomass by enzymatic hydrolysis I a simple method for isolating β-D-mannanase-produeing microorganisms [J]. Mokuzai Gakkaishi, 1992,38(12):1126-1135.
  • 6Takahashi R, Kusakabe I, Maekawa A. Studies on mannanase of Actinomycetes [J]. Tropic Agricultural, 1983,27(3):140-148.
  • 7Kurakake M, Komaki T. Production of β-mannanase and β-mannosidase form Aspergillus awamori K4 and their properties[J]. Current Microbiology,2001,2:377-380.
  • 8Waine M, Ingvorsen K. Production of halostable β-mannanase and β-mannosidase by strain NN, a new extremely halotolerant bacterium[J]. Applied Microbiology Biotechnology, 1999, 52:675-680.
  • 9Bailey M J, Beily P, Poutanen K. Interlaboratory testing of methods for assay of xylannase activity[J]. Journal of Biotechnology, 1992, 23:257-270.
  • 10Gray L, Peterson. Review of the Folin phenol protein quantitation method of Lowry, Rosebrough, Farr and Randall[J]. Analytical Biochemistry, 1979,100: 201-220.

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