期刊文献+

尿苷肽类抗生素sansanmycin D的分离、纯化和结构鉴定 被引量:3

Isolation,purification and structure determination of uridylpeptide antibiotic sansanmycin D with activity against Pseudomonas aeruginosa
下载PDF
导出
摘要 目的从尿苷肽类抗生素sansanmycins的产生菌Streptomyces sp.SS的发酵液中分离、提取和纯化小组分,并进行结构鉴定。方法以铜绿假单胞菌为检定菌,利用大孔树脂吸附、反相制备HPLC等方法进行分离纯化。用光谱分析,进行结构解析。结果分离到一个尿苷肽类化合物sansanmycin D。结论Sansanmycin D与文献报道的mureidomycin A结构一致。 Objective To isolate and purify the minor components from the fermentation broth of Strepto-myces sp. SS producing sansanmycins and determine their structures. Method Antibiotic activity was determined by a paper-disc agar diffusion assay using Pseudomonas aeruginosa. The active antibiotics were isolated and purified by means of various chromatographies, such as macroporous adsorption resins, reversed-phase HPLC, etc. Their struc-tures were elucidated by spectroscopic analyses. Result A uridylpeptide antibiotic sansanmycin D was obtained. Conclusion Sansanmycin D was designated as mureidomycin A.
出处 《中国抗生素杂志》 CAS CSCD 北大核心 2009年第1期12-14,44,共4页 Chinese Journal of Antibiotics
关键词 Sansanmycin D 尿苷肽 铜绿假单胞菌 Sansanmycin D Uridylpeptides Pseudomonas aeruginosa
  • 相关文献

参考文献10

  • 1Dini C. MraY inhibitors as novel antibacterial agents[J]. Curr Top Med Chem, 2005, 5 (13): 1221 - 1236.
  • 2Xie Y Y, Chen R X, Si S Y, etal. A new nucleosidyl-peptide antibiotic, Sansanmycin[J]. J Antibiot, 2007, 60(2): 158-161.
  • 3Xie Y Y, Xu H Z, SiS Y, et al. Sansanmycins Band C, new components of Sansanmycins[J]. J Antibiot, 2008, 61 (4): 237-240.
  • 4Karwowski J P, Jackson M, Theriault R J, et al. Pacidamycins, a novel series of antibiotics with anti-Pseudomonas aeruginosa activity. I. Taxonomy of the producing organism and fermentation[J]. J Antibiot, 1989, 42(4):506 -511.
  • 5Chen R H, Buko A M, Whittern D N, et al. Pacidamycins, a novel series of antibiotics with anti-Pseudomonas aeruginosa activity. Ⅱ. Isolation and structural elucidation[J]. J Antibiot, 1989, 42(4): 512 -520.
  • 6Fronko R M, Lee J C, Galazzo J G, et al. New pacidamycins produced by Streptomyces coeruleorubidus, NRRL 18370[J]. J Antibiot, 2000, 53(12): 1405-1410.
  • 7Inukai M, Isono F, Takahashi S, et al. Mureidomycins A-D, novel peptidylnucleoside antibiotics with spheroplast forming activity.Ⅰ. Taxonomy, fermentation, isolation and physi- co-chemical properties[J]. J Antibiot, 1989, 42(5): 662 -666.
  • 8Isono F, Inukai M, Takahashi S, et al. Mureidomycins A-D, novel peptidylnucleoside antibiotics with spheroplast forming activity. Ⅱ. Structural elucidation[J]. J Antibiot, 1989, 42 (5): 667 - 673.
  • 9Isono F, Sakaida Y, Takahashi S, et al. Mureidomyeins E and F, minor components of mureidomycins[J]. J Antibiot, 1993, 46 (8): 1203- 1207.
  • 10Chatterjee S, Nadkarni S R, Vijayakumar E K, et al. Napsamyeins, new Pseudomonas active antibiotics of the mureidomycin family from Streptomyces sp. HIL Y-82, 11372[J]. J Antibiot, 1994, 47 (5): 595-598.

同被引文献6

  • 1Dini C.Mra Y inhibitors as novel antibacterial agents[J].Cur ropi Med Chemi,2005,5(13):1221-1236.
  • 2Xie Y Y,Chen R X,Si S Y,et al.A new nucleosidyl-peptide antibiotic,Sansanmycin[J].J Antilbiot,2007,60(2):158-161.
  • 3Xie Y Y,Xu H Z,Si S Y,Sun C H,et al.Sansanmycins B and C,new components of sansanmycins[J].J Antibiot,2008,61(4):237-240.
  • 4Kikuchi Y,Tamiya N,Nozawa T,et al.Non-destructive detection of methionine sulfoxide in the resilium of a surf clam by solid-state ^13C-NMR spectroscopy[J].Eur J Biochem,1982,125(3):575-577.
  • 5解云英,许鸿章,俞莹,陈汝贤.尿苷肽类抗生素sansanmycin E的分离、纯化和结构鉴定[J].中国抗生素杂志,2009,34(6):326-328. 被引量:3
  • 6李青连,解云英,王丽非,许鸿章,陈汝贤,洪斌.尿苷肽类抗生素生物合成研究进展[J].国际药学研究杂志,2012,39(1):17-25. 被引量:2

引证文献3

二级引证文献3

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