期刊文献+

非离子表面活性剂对鞘氨醇单胞菌MH13转化吩嗪的影响

Effect of Nonionic Surfactants on the Biotransformation of Phenazine by Sphingobium sp. MH13
下载PDF
导出
摘要 1,2-二羟基-1,2-二氢吩嗪是一种手性的二醇,可以被用来作为合成吩嗪类衍生物的前体。鞘氨醇单胞菌MH13能将吩嗪转化为1,2-二羟基-1,2-二氢吩嗪。利用添加非离子表面活性剂的方法对鞘氨醇单胞菌MH13转化吩嗪进行了研究。首先考察了不同种类的非离子表面活性剂对菌株生长的影响。结果表明2%的Triton X-100和Triton X-114抑制鞘氨醇单胞菌MH13的生长,而2%的聚醚L64对鞘氨醇单胞菌MH13毒性较小。然后选用2%的聚醚L64作为添加剂,在培养24h后中间产物1,2-二羟基-1,2-二氢吩嗪产量达到最大,浓度达到了(98.9±7.1)mg/L,是不添加非离子表面活性剂的1.32倍。 1,2-Dihydroxy-1,2-dihydrophenazine(DHDP)is a kind of chiral diol which can be used as a precursor for synthesizing phenazine derivatives.Sphingobiumsp.MH13 can transform phenazine to 1,2-dihydroxy-1,2-dihydrophenazine.The effect of nonionic surfactants on the biotransformation of phenazine by sphingobiumsp.MH13 was investigated.Firstly,the effects of different kinds of nonionic surfactant on cell growth were studied.The result showed that the addition of 2% Triton X-100 and Triton X-114 inhibited the growth of sphingobiumsp.MH13,while 2% polyether L64 showed little toxicity to sphingobium sp.MH13.Then polyether L64 was selected as the additive for the biotransformation of phenazine.After adding 2% concentration of polyether L64 for 24h,the production of DHDP reached the maximum as(98.9±7.1)mg/L,which was 1.32 times more than that of the control.
出处 《化学世界》 CAS CSCD 2016年第6期375-379,共5页 Chemical World
基金 国家自然科学基金(21377082和J1210047)
关键词 鞘氨醇单胞菌 非离子表面活性剂 1 2-二羟基-1 2-二氢吩嗪 吩嗪 sphingomonas nonionic surfactant 1 2-dihydroxy-1 2-dihydrophenazine phenazine
  • 相关文献

参考文献13

  • 1MAVRODI D V, BONSALL R F, DELANEY S M, et al. Functional Analysis of Genes for Biosynthesis of Pyocyanin and Phenazine-l-carboxamide from Pseudo- monas Aeruginosa PAO1 [J]. Int J Bac,2001,183(21) .. 6 454-6 465.
  • 2CHIN-A-WOENG T F C, BLOEMBERG G V, van der BIJ A J,et al. Biocontrol by Phenazine-l-earbox- amide-producing Pseudomonas Chlororaphis PCL1391 of Tomato Root Rot Caused by Fusarium Oxysporum f. sp. Radicis-lycopersici [J]. Mol Plant-Microbe Int, 1998,11(11):1 069-1 077.
  • 3PRICE-WHELAN A,DIETRICH L E P, NEWMAN D K. Rethinking ' Secondary' Metabolism: Physio- logical Roles for Phenazine Antibiotics [J]. Nat Chem Biol, 2006,2 (2) : 71-78.
  • 4LAURSEN J B, NIELSEN J. Phenazine Natural Products : Biosynthesis, Synthetic Analogues, and Bio- logical Activity [J]. Chem Rev, 2004, 104(3).. 1 663-1 686.
  • 5MCDONALD M, MAVRODI D V, THOMASHOW L S, et al. Phenazine Biosynthesis in Pseudomonas Fluorescens:Branchpoint from the Primary Shikimate Biosynthetic Pathway and Role of Phenazine-1,6-Di- carboxylic Acid [J]. J Am Chem Soc,2001,123(38) : 9 459-9 460.
  • 6BRISBANE P G,JANIK L J,TATE M E,et al. Re- vised Structure for the Phenazine Antibiotic from Pseudomonas Fluorescens 2-79 (NRRL B-15132 ) [J]. An Agen Chem,1987,31(12):1 967-1 971.
  • 7MAVRODI D V, KSENZENKO V N, BONSALL R F,et al. A Seven-gene Locus for Synthesis of Phena- zine-1-carboxylic Acid by Pseudomonas Fluorescens 2- 79 [J]. Int, J Bac,1998,180(9):2 541-2 548.
  • 8WILKES H,WITTICH R,TIMMIS K,et al. Degra- dation of Chlorinated Dibenzofurans and Dibenzo-p- Dioxins by Sphingomonas sp. Strain RW1. [J]. Appl Env Mic,1996,62(2) : 367-371.
  • 9STOLZ A. Molecular Characteristics of Xenobiotic- degrading Sphingomonads [J]. Appl Env Mic,2009, 81(5) : 793-811.
  • 10KANG B,ZHANG X,WU Z,et al. Solubilization Ca- pacity of Nonionic Surfactant Micelles Exhibiting Strong Influence on Export of Intracellular Pigments in Monascus Fermentation [J]. Mie Bio, 2013,6 (5) : 540-550.

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