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交替假单胞菌LP621菌株产右旋糖苷酶的培养条件优化 被引量:7

Culture Optimization of Dextranase-Producing Pseudoalteromonas tetraodonis LP621
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摘要 从江苏连云港海域分离和筛选到1株产右旋糖苷酶的海洋细菌交替假单胞菌Pseudoalteromonas tetraodonis LP621,通过单因素试验和正交试验对该菌株产右旋糖苷酶培养条件进行优化。单因素试验结果表明,最佳培养时间为24 h,最适产酶温度为25℃;产酶pH范围为5.0~11.0,最适产酶pH为6.0;产酶NaCl浓度范围为1%~10%,NaCl浓度为4%时产酶较高;装液量在25%。麦芽糖、胰蛋白胨和酵母膏促进产酶。利用响应面方法对LP621产右旋糖苷酶的发酵条件进行优化。选择培养基pH、时间、麦芽糖浓度和装液量4因素进行优化,结果为pH 7.07,发酵时间21.94 h,麦芽糖浓度0.42%,装液量为21.88%,酶活为270.1U/mL。 A dextranse-producing marine bacteria Pseudoalteromonas tetraodonis LP621 was screened and isolated from the sea area of Lianyungang,Jiangsu.Its dextranase production conditions was optimized through single-factor and orthogonal experiments.The results of single factor experiment indicated that the most suitable culture condition was 24 hours,and the most suitable dextranse producing temperature was 25 ℃ at pH 6.0 with ranging 5.0~11.0,and the range of the concentration of NaCl for the dextranse production was 1%~10%,and the yield of dextranase was fairly high at 4% of NaCl with filling volume rate at 25%.Maltose,tryptone,and yeast extract enhanced the enzyme production.Response surface method was adopted to optimize the enzyme production fermentation conditions.Medium pH,time,maltose,and filling volume four factors were selected for the optimization.And the results were pH 7.07,21.94 h,maltose 0.42%,and filling volume 21.88%,the enzyme activity was 270.1 U/mL.
出处 《微生物学杂志》 CAS CSCD 2010年第6期11-17,共7页 Journal of Microbiology
基金 国家自然科学基金(40746030) 江苏省科技厅工业支撑计划项目(BE2009095) 江苏省海洋生物技术重点建设实验室开放课题项目(2008HS008) 连云港市自然科学基金(ZH200801)
关键词 右旋糖苷酶 交替假单胞菌属 优化 dextranase Pseudoalteromonas tetradonis optimization
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  • 1Khalikova E, Susi P, Usanov N, et al. Purification and properties of extracellular dextranase from a Bacillus sp. [J]. J. Chroma- togr B, 2003,796 (2) :315-326.
  • 2Khalikova E, Susi P, Korpela T. Microbial dextran-hydrolyzing enzymes:fundamentals and applications[J]. M icrobiol Mol Biol Rev,2005,69(2) :306-325.
  • 3Asian Y,Tanriseven A. Immobilization of Penicillium lilacinum dextranase to produce isomahooligosaccharides from dextran [J]. Biochem Eng,J,2007,34(1) :8-12.
  • 4Chen L,Zhou X,Fan W,Zhang Y,et al. Expression, purifica- tion and characterization of a recombinant Lipomyces starkey dextranase in Pichia pastoris [J]. Protein Expr Purif, 2008,58 (1) :87-93.
  • 5Hattori A, Ishibashi K, Minato S. The purification and charac- terization of the dextranse of Chaetomium gracile [J]. Agri Bio Chem, 1981,45 (11) :2409-2416.
  • 6程秀兰,孙晋武,王海燕,严自正,张树政.焦曲霉右旋糖酐酶的纯化和性质[J].微生物学报,1992,32(3):218-226. 被引量:5
  • 7Kim Y M,Seo M Y,Kang H K,et al. Construction of a fusion enzyme of dextransucrase and dextranase: Application for one-step synthesis of isomalto-oligosaecharides [J].Enzy Micro Teeh, 2009,44(3) :159-164.
  • 8Gauthier G, Gauthier M, Christen R. Phylogenetie analysis of the genera Alteromonas, Shewanella, and Morltella using genes coding for small-subunit rRNA sequences and division of thegenus Alteromonas into two genera,Alteromonas (emended) and Pseudoalteromonas gen. nov,and proposal of twele new species combinations[J]. Int J Syst Bacteriol, 1995,45:755-761.
  • 9Carolina CR, Rowley AF. Effect of extracellular products of Pseudoalteromonas atlantiea on the edible crab Cancer pagurus [J]. Appl Environ Microbiol,2004,70(2) :729-735.
  • 10Park YD, Baik KS, Yi H, et al. Pseudoalteromanas byunsanensis sp. nov. , isolated from tidal flat sediment in Korea[J]. Int J Syst Evol Mierebiol,2005 ,55 :2519-2523.

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