Dereplication of Streptomyces sp. AMC 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry.

Abstracts: Actinomycetes, especially those belonging to the genus Streptomyces, are economically important from a biotechnological standpoint: they produce antibiotics, anticancer compounds and a variety of bioactive substances that are potentially applicable in the agrochemical and pharmaceutical industries. This paper combined accurate-mass electrospray tandem mass spectrometry in the full scan and product ion scan modes with compounds library data to identify the major compounds in the crude extract produced by Streptomyces sp. AMC 23; it also investigated how sodiated nonactin ([M + Na]+) fragmented. Most product ions resulted from elimination of 184 mass units due to consecutive McLafferty-type rearrangements. The data allowed identification of four macrotetrolides homologous to nonactin (monactin, isodinactin, isotrinactin/trinactin and tetranactin) as well as three related linear dimer compounds (nonactyl nonactoate, nonactyl homononactoate and homononactyl homononactoate). The major product ions of the sodiated molecules of these compounds also originated from elimination of 184 and 198 mass units. UPLC-MS/MS in the neutral loss scan mode helped to identify these compounds on the basis of the elimination of 184 and 198 mass units. This method aided monitoring of the relative production of these compounds for 32 days and revealed that the biosynthetic process began with increased production of linear dimers as compared with macrotetrolides. These data could facilitate dereplication and identification of these compounds in other microbial crude extracts.

Saved in:
Bibliographic Details
Main Authors: CREVELIN, E. J., CROTTI, A. E. M., ZUCCHI, T. D., MELO, I. S. de, MORAES, L. A. B.
Other Authors: EDUARDO JOSE CREVELIN, FFCLRP-USP; ANTONIO EDUARDO MILLER CROTTI, FFCLRP-USP; TIAGO DOMINGUES ZUCCHI, FAPESP; ITAMAR SOARES DE MELO, CNPMA; LUIZ ALBERTO BERALDO MORAES, FFCLRP-USP.
Format: Separatas biblioteca
Language:English
eng
Published: 2014-12-23
Subjects:Macrotetrolides, Actinomycetes, UPLC-MS/MS, Nonactic acid, Actinomiceto, Espectrometria, Streptomyces, Actinomycetales, DNA fragmentation, Extracts, Ultra-performance liquid chromatography, Tandem mass spectrometry,
Online Access:http://www.alice.cnptia.embrapa.br/alice/handle/doc/1003573
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-alice-doc-1003573
record_format koha
spelling dig-alice-doc-10035732017-08-16T01:39:23Z Dereplication of Streptomyces sp. AMC 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry. CREVELIN, E. J. CROTTI, A. E. M. ZUCCHI, T. D. MELO, I. S. de MORAES, L. A. B. EDUARDO JOSE CREVELIN, FFCLRP-USP; ANTONIO EDUARDO MILLER CROTTI, FFCLRP-USP; TIAGO DOMINGUES ZUCCHI, FAPESP; ITAMAR SOARES DE MELO, CNPMA; LUIZ ALBERTO BERALDO MORAES, FFCLRP-USP. Macrotetrolides Actinomycetes UPLC-MS/MS Nonactic acid Actinomiceto Espectrometria Streptomyces Actinomycetales DNA fragmentation Extracts Ultra-performance liquid chromatography Tandem mass spectrometry Abstracts: Actinomycetes, especially those belonging to the genus Streptomyces, are economically important from a biotechnological standpoint: they produce antibiotics, anticancer compounds and a variety of bioactive substances that are potentially applicable in the agrochemical and pharmaceutical industries. This paper combined accurate-mass electrospray tandem mass spectrometry in the full scan and product ion scan modes with compounds library data to identify the major compounds in the crude extract produced by Streptomyces sp. AMC 23; it also investigated how sodiated nonactin ([M + Na]+) fragmented. Most product ions resulted from elimination of 184 mass units due to consecutive McLafferty-type rearrangements. The data allowed identification of four macrotetrolides homologous to nonactin (monactin, isodinactin, isotrinactin/trinactin and tetranactin) as well as three related linear dimer compounds (nonactyl nonactoate, nonactyl homononactoate and homononactyl homononactoate). The major product ions of the sodiated molecules of these compounds also originated from elimination of 184 and 198 mass units. UPLC-MS/MS in the neutral loss scan mode helped to identify these compounds on the basis of the elimination of 184 and 198 mass units. This method aided monitoring of the relative production of these compounds for 32 days and revealed that the biosynthetic process began with increased production of linear dimers as compared with macrotetrolides. These data could facilitate dereplication and identification of these compounds in other microbial crude extracts. 2014-12-23T11:11:11Z 2014-12-23T11:11:11Z 2014-12-23 2014 2014-12-23T11:11:11Z Separatas Journal of Mass Spectrometry, Chichester, v. 49, n. 11, p. 1117-1126, 2014. http://www.alice.cnptia.embrapa.br/alice/handle/doc/1003573 en eng openAccess
institution EMBRAPA
collection DSpace
country Brasil
countrycode BR
component Bibliográfico
access En linea
databasecode dig-alice
tag biblioteca
region America del Sur
libraryname Sistema de bibliotecas de EMBRAPA
language English
eng
topic Macrotetrolides
Actinomycetes
UPLC-MS/MS
Nonactic acid
Actinomiceto
Espectrometria
Streptomyces
Actinomycetales
DNA fragmentation
Extracts
Ultra-performance liquid chromatography
Tandem mass spectrometry
Macrotetrolides
Actinomycetes
UPLC-MS/MS
Nonactic acid
Actinomiceto
Espectrometria
Streptomyces
Actinomycetales
DNA fragmentation
Extracts
Ultra-performance liquid chromatography
Tandem mass spectrometry
spellingShingle Macrotetrolides
Actinomycetes
UPLC-MS/MS
Nonactic acid
Actinomiceto
Espectrometria
Streptomyces
Actinomycetales
DNA fragmentation
Extracts
Ultra-performance liquid chromatography
Tandem mass spectrometry
Macrotetrolides
Actinomycetes
UPLC-MS/MS
Nonactic acid
Actinomiceto
Espectrometria
Streptomyces
Actinomycetales
DNA fragmentation
Extracts
Ultra-performance liquid chromatography
Tandem mass spectrometry
CREVELIN, E. J.
CROTTI, A. E. M.
ZUCCHI, T. D.
MELO, I. S. de
MORAES, L. A. B.
Dereplication of Streptomyces sp. AMC 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry.
description Abstracts: Actinomycetes, especially those belonging to the genus Streptomyces, are economically important from a biotechnological standpoint: they produce antibiotics, anticancer compounds and a variety of bioactive substances that are potentially applicable in the agrochemical and pharmaceutical industries. This paper combined accurate-mass electrospray tandem mass spectrometry in the full scan and product ion scan modes with compounds library data to identify the major compounds in the crude extract produced by Streptomyces sp. AMC 23; it also investigated how sodiated nonactin ([M + Na]+) fragmented. Most product ions resulted from elimination of 184 mass units due to consecutive McLafferty-type rearrangements. The data allowed identification of four macrotetrolides homologous to nonactin (monactin, isodinactin, isotrinactin/trinactin and tetranactin) as well as three related linear dimer compounds (nonactyl nonactoate, nonactyl homononactoate and homononactyl homononactoate). The major product ions of the sodiated molecules of these compounds also originated from elimination of 184 and 198 mass units. UPLC-MS/MS in the neutral loss scan mode helped to identify these compounds on the basis of the elimination of 184 and 198 mass units. This method aided monitoring of the relative production of these compounds for 32 days and revealed that the biosynthetic process began with increased production of linear dimers as compared with macrotetrolides. These data could facilitate dereplication and identification of these compounds in other microbial crude extracts.
author2 EDUARDO JOSE CREVELIN, FFCLRP-USP; ANTONIO EDUARDO MILLER CROTTI, FFCLRP-USP; TIAGO DOMINGUES ZUCCHI, FAPESP; ITAMAR SOARES DE MELO, CNPMA; LUIZ ALBERTO BERALDO MORAES, FFCLRP-USP.
author_facet EDUARDO JOSE CREVELIN, FFCLRP-USP; ANTONIO EDUARDO MILLER CROTTI, FFCLRP-USP; TIAGO DOMINGUES ZUCCHI, FAPESP; ITAMAR SOARES DE MELO, CNPMA; LUIZ ALBERTO BERALDO MORAES, FFCLRP-USP.
CREVELIN, E. J.
CROTTI, A. E. M.
ZUCCHI, T. D.
MELO, I. S. de
MORAES, L. A. B.
format Separatas
topic_facet Macrotetrolides
Actinomycetes
UPLC-MS/MS
Nonactic acid
Actinomiceto
Espectrometria
Streptomyces
Actinomycetales
DNA fragmentation
Extracts
Ultra-performance liquid chromatography
Tandem mass spectrometry
author CREVELIN, E. J.
CROTTI, A. E. M.
ZUCCHI, T. D.
MELO, I. S. de
MORAES, L. A. B.
author_sort CREVELIN, E. J.
title Dereplication of Streptomyces sp. AMC 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry.
title_short Dereplication of Streptomyces sp. AMC 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry.
title_full Dereplication of Streptomyces sp. AMC 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry.
title_fullStr Dereplication of Streptomyces sp. AMC 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry.
title_full_unstemmed Dereplication of Streptomyces sp. AMC 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry.
title_sort dereplication of streptomyces sp. amc 23 polyether ionophore antibiotics by accurate-mass electrospray tandem mass spectrometry.
publishDate 2014-12-23
url http://www.alice.cnptia.embrapa.br/alice/handle/doc/1003573
work_keys_str_mv AT crevelinej dereplicationofstreptomycesspamc23polyetherionophoreantibioticsbyaccuratemasselectrospraytandemmassspectrometry
AT crottiaem dereplicationofstreptomycesspamc23polyetherionophoreantibioticsbyaccuratemasselectrospraytandemmassspectrometry
AT zucchitd dereplicationofstreptomycesspamc23polyetherionophoreantibioticsbyaccuratemasselectrospraytandemmassspectrometry
AT meloisde dereplicationofstreptomycesspamc23polyetherionophoreantibioticsbyaccuratemasselectrospraytandemmassspectrometry
AT moraeslab dereplicationofstreptomycesspamc23polyetherionophoreantibioticsbyaccuratemasselectrospraytandemmassspectrometry
_version_ 1756020305016389632