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一株产冠毒素新菌株发酵条件的初步研究 被引量:4

A Study on Fermentation Condition for a New Coronatine-producing Strain Y57
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摘要 通过对产冠毒素新菌株洋葱假单胞菌Pseudomonas cepacia Y57培养温度和时间的研究,发现菌株Y57在碳源充足的情况下,不同培养温度对菌株的生长影响不明显,但影响菌株的产素能力,以32~18℃的变温培养为佳;接着运用正交试验确定了菌株的最佳培养基配方,即:葡萄糖(20g/L),蛋白胨(1.5g/L),FeCl3(15μmol/L),KH2PO4(4.0g/L),K2HPO4(1.8g/L),MgSO4·7H2O(0.2g/L);最后根据试验结果,确定了摇瓶发酵的最适条件为:采用最佳培养基配方,32℃培养1d,降温至18℃发酵2d,冠毒素的效价由优化前的98μg/mL提高到128μg/mL,提高了30%左右。 An experiment was conducted to study the effect of fermentation temperature and time on growth and coronatine production of Pseudomonas cepacia strain Y57. The result revealed that in contrast with the change of growth, the difference of coronatine production was noticeable under different culture temperatures for strain Y57 when the carbon source was sufficient, and the optimum fermentation temperature range was from 32 ℃ to 18 ℃. The orthogonal experiment result suggested that the suitable medium for coronatine produced by strain Y57 during shake-flask fermentation are as follows: glucose(20 g/L), peptone( 1.5 g/ L), MgSO4 ·7H2O (0.2g/L),FeC13(15 μmol/L), KH2PO4(4.0 g/L) , K2HPO4(1.8 g/L). In conclusion, the optimum fermentation conditions are: viz. fermentating 3 d, temperature from 30 ℃ ld to 18 ℃ 2 d, the suitable medium aforementioned. Under these conditions the yield of coronatine was increased by about 30% from 98 μg/mL to 128 μg/mL.
出处 《江西农业大学学报》 CAS CSCD 北大核心 2006年第4期592-597,共6页 Acta Agriculturae Universitatis Jiangxiensis
基金 国家自然科学基金(30360050) 江西省自然科学基金(0230043)资助项目
关键词 洋葱假单胞菌Y57 冠毒素 发酵条件 优化 Pseudomonas cepacia strain Y57 coronatine fermentation condition optimum
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参考文献11

  • 1吴晓玉,储炬,曾晓春.冠毒素生物合成与调控的研究进展[J].天然产物研究与开发,2005,17(1):98-103. 被引量:6
  • 2Weiler E W,Kutchan T M,Gorba T,et al.The Pseudomonas phytotoxin coronatine mimics octadecanoid signaling molecules of higher plants[J].FEBS Lett,1994,345:9-13.
  • 3Vignutelli A,Wasternack C,Apel K,et al.Systemic and local induction of an Arabidopsis thionin gene by wounding and pathogens[J].Plant J,1998,14:285-295.
  • 4Koda Y,Takahashi K,Kikuta Y,et al.Similarities of the biological activities of coronatine and coronafacic acid to those of jasmonic acid[J].Phytochemistry,1996,41:93-96.
  • 5Gnanamaickam S S,Starratt A N,Ward E W B.Coronatine production in vitro and in vivo and its relation to symptom development in bacterial blight of soybean[J].Can J Bot,1982,60:645-650.
  • 6Friedemann Greulich,Terubiko Yoshihara,Akitarci Ichihata.Coronatine,abacterial phyrotoxin,acts as a sreteospenfic analog of jasmonate type signals in tomato ceils and potato tissue[J].J Plant Physio,1995,147:359-366.
  • 7曾晓春,周燮,吴晓玉.水稻颖花开放机理研究进展[J].中国农业科学,2004,37(2):188-195. 被引量:49
  • 8Ullrich M,Pealoza-Vázquez A,Bailey AM,et al.A modified two-component regulatory system is involved in temperature-dependent biosynthesis of the Pseudomonas syringae phytotoxin coronatine[J].J Bacteriol,1995,177:6 160-6 169.
  • 9David A Palmer,Carol L.Bender,Effects of Environmental Factors on Production of the Polyketide Phytoto -zxin Coronatine by Pseudomonas syringae pv.Glycinea[J].Applied and Enviroment Microbiology,1993:1 619 -1 625.
  • 10李永华.农业应用生物统计[M].第1版.济南:山东科学技术出版社,1989:328-346.

二级参考文献74

  • 1玉忠,顾蕴洁,高煜珠.水稻开颖机理的探讨——Ⅱ.CO_2对水稻开颖的效应[J].作物学报,1989,15(1):59-66. 被引量:34
  • 2王忠.CO2促进水稻开花的效应[J].植物生理学通讯,1987,(3):29-29.
  • 3Rohde BH, Pohlack B, Ullrich MS. Occurrence of thermoregulation of genes involved in coronatine biosynthesis among various Pseudomonas syringae strains. J Basic Microbiol, 1998,38:41-50.
  • 4Ullrich M, Penaloza-Vazquez A, Bailey AM, et al. A modified two-component regulatory system is involved in temperature-dependent biosynthesis of the Pseudomonas syringae phytotoxin coronatine. J Bacteriol , 1995,177:6160-6169.
  • 5Wang L, Bender CL, Ullrich MS. The transcriptional activator CorR is involved in biosynthesis of the phytotoxin cororatine and binds to the cmaABT promoter region in a temperattre-dependent manner. Mol Gen Genet , 1999,262(2):250-260.
  • 6Smirnova AV, Wang L, Rohde B, et al. Control of temperatureresponsive synthesis of the phytotoxin coronatine in Pseudomonas syringae by the tnconventional two-component system CorRPS. J Mol Microbiol Biotechnol, 2002,4(3): 191-6.
  • 7Alarcon-Chaidez FJ, Keith L, Zhao Y, et al. RpoN(sigma(54))is required for plasmid-encoded coronatine biosynthesis in Pseudomonas syringae. Plasmid,2003,49(2):106-117.
  • 8Hendrickson EL, Guevera P, Penaloza-Vazquez A, et al. Virulence of the phytopathogen Pseudomonas syringae pv. Maculicola is rpoN dependent. J Bacteriol,2000,182(12) :3498-3507.
  • 9Penaloza-Vazquez A, Preston GM, Collmer A, et al. Regulatory interactions between the Hrp type Ⅲ protein secretion system and cororatine biosynthesis in Pseudomonas syringae pv. tomato DC3000. Microbiology, 2000, 146: 2447-2456.
  • 10Cuppels DA, Ainsworth T. Molecular and physiological characterization of Pseudomonas syringae pv. tomato and Pseudomonas syringae pv. Maculicola strains that produce the phytotoxin coronatine. Appl Environ Microbiol , 1995,61 (10): 3530-3536.

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