期刊文献+

枯草杆菌Bacillus sp F26产过氧化氢酶的发酵条件 被引量:2

Optimization of Catalase Production with a Halophilic and Alkaliphilic Bacterium Bacillus sp F26
在线阅读 下载PDF
导出
摘要 从内蒙古呼伦贝尔草原的盐碱湖中分离到的一株低度嗜盐嗜碱细菌Bacillus sp F26,能积累高水平过氧化氢酶(CAT)。对Bacillus sp F26发酵产过氧化氢酶的环境与营养条件的研究结果表明,其积累高水平过氧化氢酶的适宜环境条件为:温度37℃,种龄20-22h,接种量5%,装液量50mL/(250mL的摇瓶)。适宜发酵培养基组成(g/L)为:葡萄糖15,牛肉膏10,玉米浆10,酵母膏5,磷酸二氢钾1,氯化镁0.2,氯化钠50,碳酸钠10。采用上述条件进行摇瓶分批发酵实验,发酵20h,过氧化氢酶酶活达到16.32U/mL,细胞干重为4.12g/L。进一步研究发现,在对数生长后期(16h)添加2mmol/L的H2O2可以明显刺激产酶,在5L的发酵罐上进一步以指数速率方式流加H2O2,由于该流加方式可降低H2O2对细胞的毒害作用,过氧化氢酶酶活达到29.89U/mL,与分批发酵相比提高了92.8%。 The effects of culture conditions and medium compositions on the fermentative production of catalase (CAT) by a slight halophilic and alkaliphilic bacterium Bacillus sp F26, isolated from Haoji Soda Lake, P. R China, were investigated. The optimal culture conditions were obtained as following, temperature 37 ℃, age seed 20-22 h , inoculum size 5% and volume 50 mL in 250 mL shaking-flask. The optimal fermentation medium contained 15 g/L of glucose, 10 g/L of beef extract, 10 g/L of corn liquid, 5 g/L of yeast extract, 1 g/L of KH2PO4, 0. 2 g/L of MgCl2, 50 g/L of NaCl and 10 g/L of Na2CO3. High CAT activity (16.32 U/mL) and dry cell weight (4. 12 g/L) were observed at 20 h in shaking-flask culture. It was also found that addition of H2O2(2 mmoL/L in the medium) at later exponential phase greatly induced the synthesis of CAT. The maximum CAT activity (29.89 U/mL) was obtained by using exponential H2O2 feeding strategy in 5 L fermentor, which was 92.8% higher than that in batch fermentation.
出处 《食品与生物技术学报》 CAS CSCD 北大核心 2007年第1期77-83,共7页 Journal of Food Science and Biotechnology
基金 国家自然科学基金资助项目(20676056) 国家高技术研究发展计划(863)资助项目(No.2003AA322050) 江苏省创新人才(学术)基金资助项目(BK2004401)
关键词 低度嗜盐嗜碱细菌 BACILLUS SP F26 过氧化氢酶 发酵优化 过氧化氢 指数速率流加 Bacillus sp F26 catalase optimazation of fermentation hydrogen-peroxide exponential fed-batch model
  • 相关文献

参考文献16

  • 1Farr S,Kogoma T.Oxidative stress response in Escherichia coil and Salmonella typhimurium[J].Microbiol Rev,1991,55(4):561-585.
  • 2Allgod GS,Perry JJ.Characterization of a manganese-containing catalase from the obligate thermophile Thermoleophilum album[J].J Bacteriol,1986,168(2):563-567.
  • 3Isao Y,Yoshihiro F,Tateo Y.Purification and characterization of catalase from a facultative alkalophilic Bacillus[J].J Biochem,1990,108:583-587.
  • 4Parr A,Cosat S,Tzanov T,et al.Thermo-alkali-stable catalases from newly isolated Bacillus sp.for the treatment and recycling of textile bleaching effluents[J].J Biotechnol,2001,89:147-153.
  • 5张心齐,薛燕芬,赵爱民,堵国成,许正宏,陈坚,马延和.嗜碱芽孢杆菌Bacillus sp.F26过氧化氢酶的分离纯化及性质研究(英文)[J].生物工程学报,2005,21(1):71-77. 被引量:9
  • 6Bergmeger Hu,Bergmeyer J,Grabl M,et al.Methods of Enzymatic Analysis[M].Weinheim:Verlag Chemie Press,1983.
  • 7Miller G L.Dinitrosalicylic acid reagent for determination of reducing sugar[J].Anal Chem,1960,31:426-428.
  • 8Shiraishi F,Nakasako T,Hua Z Z.Formation of hydrogen peroxide in photocatalytic reactions[J].J Phys Chem A,2003,(107):11072-11081.
  • 9Hassan H M,Fridovich I.Regulation of the synthesis of catalase and peroxidase in Escherichia coli[J].J Biol Chem,1978,253(8):6445-6450.
  • 10Terzenbach D P,Blaut M.Purification and characterization of a catalase from the nonsulfur phototrophic bacterium Rhodobacter sphaeroides ATH 2.4.2 and its role in the oxidative stress response[J].Arch Microbiol,1998,169:503-508.

二级参考文献30

  • 1Hartford OM, Dowds DC. Isolation and characterization of a hydrogen peroxide resistant mutant of Bacillus subtilis. Microbiololgy,1994, 140: 297- 304.
  • 2Shima S, Netrusov A, Sordel M et al. Purification, characterization, and primary structure of a monofunctional catalase from Methanosarcina barkeri . Arch Microbiol , 1999, 171:317-323.
  • 3Thompson VS, Schaller KD, Apel WA. Purification and characterization of a noval thermo-alkali-stable catalase from Thermus brockianus. Biotechnol Prog., 2003, 19: 1292- 1299.
  • 4Phucharoen K, Hoshino K, Takenaka Y et al. Purification, characterization, and gene sequencing of a catalase from an alkali- and halo-tolerant bacterium, Halomonas sp. SK1. Biosci Biotechnol Biochem, 2002, 66: 955- 962.
  • 5Wang HX, Tokusige Y, Shinoyama H et al. Purification and characterization of a thermostable catalase from culture broth of Thermoascus aurantiacus. Journal of Fermentation and Bioengineering,1998, 85: 169- 173.
  • 6Yumoto I, Yamazaki K, Kawasaki K et al. Isolation of Vibrio sp.S-1 exhibiting extraordinarily high catalase activity, Journal of Fermentation and Bioengineering, 1998, 85: 113 - 116.
  • 7Yumoto I, Yamazaki K, Kawasaki K et al. Isolation of Vibrio sp.S-1 exhibiting extraordinarily high catalase activity. Journal of Fermentation and Bioengineering, 1998, 85:113 - 116.
  • 8Yumoto I, Fukumori Y, Yamanaka T. Purification and characterization of catalase from a facultative alkalophilic Bacillus. J Biochem,1990, 108: 583- 587.
  • 9Hicks DB. Purification of three catalase isozymes from facultatively alkaliphilic Bacillus firmus OF4. Biochimica et Biophysica Acta,1995, 1229: 347-355.
  • 10Gudelj M, Fruhwirth GO, Paar A et al. A catalase-peroxidase from a newly isolated thermoalkaliphilic Bacillus sp. with potential for the treatment of textile bleaching effluents, Extremophiles, 2001,5: 423 - 429.

共引文献8

同被引文献29

  • 1刘冰,梁婵娟.生物过氧化氢酶研究进展[J].中国农学通报,2005,21(5):223-224. 被引量:131
  • 2王明星,李寅,方芳,华兆哲,陈坚.添加甲萘醌促进嗜热子囊菌合成过氧化氢酶[J].过程工程学报,2005,5(3):337-340. 被引量:10
  • 3段绪果,沈微,李艳丽,饶志明,唐雪明,方慧英,刘吉泉,诸葛健.耐热过氧化氢酶基因工程菌的构建及其发酵条件[J].食品与生物技术学报,2006,25(2):74-78. 被引量:8
  • 4冷晒祥,钱国坻,华兆哲,堵国成,陈坚.过氧化氢酶的棉针织物漂染工艺研究[J].印染,2006,32(19):1-3. 被引量:19
  • 5Weck M. Hydrogen peroxide-an environmentally acceptable textile bleaching agent, Text[J]. Prax is Int, 1991,46: 144- 147.
  • 6Fusho Y, Yajima Y. Catalase from Bacillus subtilis IAM 1026 (Ferm BP-4844)[P]. US Patent:5486467. 1996.
  • 7Calandrelli V, Gambacorta A, Romano I, et al. A novel thermo-alkali stablecatalase-peroxidase from Oceanobacillus oncorhynchi subsp incaldaniensis : purification and characterization[J]. World J Mierob Biot, 2008, 24 : 2269- 2275.
  • 8Nakayama M, Nakajima-Kambe T, Katayama H ,et al. High Catalase Production by Rhizobium radiobacter Strain 2-1 [J]. J Biosci Bioeng, 2008, 106 : 554- 558.
  • 9Bradford M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding[J]. Anal Biochem, 1976, 72:248- 1254.
  • 10Caridis K A, Christakopoulos P, Macris J. Simultaneous production of glucose oxidase and catalase by Alternaria alternata[J].Appl Mierobioi Bioteehnol, 1991, 34 : 794- 797.

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部