Literature DB >> 1369285

Applications of thin layer chromatography, high performance liquid chromatography and mass spectrometry in the fermentation and isolation of the antibiotic nybomycin.

J A Pope1, R A Nelson, C P Schaffner, R T Rosen, R C Pandey.   

Abstract

Thin layer chromatography (TLC), high performance liquid chromatography (HPLC) and mass spectrometry (MS) methods have been developed for the analysis of the antibiotic nybomycin, its derivatives deoxynybomycin and nybomycin acetate, during the fermentation and isolation of nybomycin. Using a quantitative HPLC based assay, the time course of nybomycin production (nybomycin titers) in 1000 liter fermentations was determined. Desorption chemical ionization mass spectrometry (DCI/MS) of standard nybomycin samples, fermentation broth samples and purified fractions suggested the co-production of deoxynybomycin which was not reported previously from this organism. TLC and HPLC were used to confirm the presence of deoxynybomycin in the crude extracts of fermentation broths.

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Year:  1990        PMID: 1369285     DOI: 10.1007/bf01576178

Source DB:  PubMed          Journal:  J Ind Microbiol        ISSN: 0169-4146


  8 in total

1.  Biological studies on the antibiotic, nybomycin.

Authors:  T D BROCK; W T SOKOLSKI
Journal:  Antibiot Chemother (Northfield)       Date:  1958-12

2.  Nybomycin: isolation, properties, and derivatives.

Authors:  T E EBLE; G A BOYACK; C M LARGE; W H DEVRIES
Journal:  Antibiot Chemother (Northfield)       Date:  1958-12

3.  NYBOMYCIN, A NEW ANTIBIOTIC WITH ANTIPHAGE AND ANTIBACTERIAL PROPERTIES.

Authors:  F Strelitz; H Flon; I N Asheshov
Journal:  Proc Natl Acad Sci U S A       Date:  1955-09-15       Impact factor: 11.205

4.  Nybomycin. 9. Synthetic and biosynthetic incorporation of 15N as a means of assigning the 13C nuclear magnetic resonance spectrum of nybomycin 1,2.

Authors:  A M Nadzan; K L Rinehart
Journal:  J Am Chem Soc       Date:  1977-07-06       Impact factor: 15.419

5.  Letter: Nybomycin. 8. Biosynthetic origin of the central ring carbons studied by 13C-labeled substrates.

Authors:  A M Nadzan; K L Rinehart
Journal:  J Am Chem Soc       Date:  1976-08-04       Impact factor: 15.419

6.  Nybomycin. VI. Incorporation of acetate- 13 C, acetate- 14 C, and methionine- 14 C.

Authors:  W M Knöll; R J Huxtable; K L Rinehart
Journal:  J Am Chem Soc       Date:  1973-04-18       Impact factor: 15.419

7.  Deoxynybomycin from a streptomyces.

Authors:  H Naganawa; T Wakashiro; A Yagi; S Kondo; T Takita
Journal:  J Antibiot (Tokyo)       Date:  1970-07       Impact factor: 2.649

8.  A new antitumor antibiotic, kazusamycin.

Authors:  I Umezawa; K Komiyama; H Oka; K Okada; S Tomisaka; T Miyano; S Takano
Journal:  J Antibiot (Tokyo)       Date:  1984-07       Impact factor: 2.649

  8 in total
  1 in total

1.  Synthetic studies on the reverse antibiotic natural products, the nybomycins.

Authors:  Oliver A Bardell-Cox; Andrew J P White; Luis Aragón; Matthew J Fuchter
Journal:  Medchemcomm       Date:  2019-05-24       Impact factor: 3.597

  1 in total

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