|
|
||||||||
Research Paper |
Dept of Plant Sciences, Montana State University, Bozeman, MT 59717, USA1
Dept of Botany and Range Sciences2 and Dept of Microbiology3, Brigham Young University, Provo, UT 84602, USA
Brigham and Womens Hospital and Harvard Medical School, Boston, MA 02115, USA4
Infectious Diseases Section, Veterans Affairs Medical Center, 500 West Fort St, Boise, ID 83702 and Dept of Medicine, University of Washington School of Medicine, Seattle, WA 98195, USA5
Novozymes Biotech Inc., 1445 Drew Ave, Davis, CA 95616, USA6
Author for correspondence: Gary Strobel. Tel: +1 406 994 5148. Fax: +1 406 994 7600. e-mail: uplgs{at}montana.edu
Munumbicins A, B, C and D are newly described antibiotics with a wide spectrum of activity against many human as well as plant pathogenic fungi and bacteria, and a Plasmodium sp. These compounds were obtained from Streptomyces NRRL 3052, which is endophytic in the medicinal plant snakevine (Kennedia nigriscans), native to the Northern Territory of Australia. This endophyte was cultured, the broth was extracted with an organic solvent and the contents of the residue were purified by bioassay-guided HPLC. The major components were four functionalized peptides with masses of 1269·6, 1298·5, 1312·5 and 1326·5 Da. Numerous other related compounds possessing bioactivity, with differing masses, were also present in the culture broth extract in lower quantities. With few exceptions, the peptide portion of each component contained only the common amino acids threonine, aspartic acid (or asparagine), glutamic acid (or glutamine), valine and proline, in varying ratios. The munumbicins possessed widely differing biological activities depending upon the target organism. For instance, munumbicin B had an MIC of 2·5 µg ml-1 against a methicillin-resistant strain of Staphylococcus aureus, whereas munumbicin A was not active against this organism. In general, the munumbicins demonstrated activity against Gram-positive bacteria such as Bacillus anthracis and multidrug-resistant Mycobacterium tuberculosis. However, the most impressive biological activity of any of the munumbicins was that of munumbicin D against the malarial parasite Plasmodium falciparum, having an IC50 of 4·5±0·07 ng ml-1. This report also describes the potential of the munumbicins in medicine and agriculture.
Keywords: endophyte, actinomycete, malaria, tuberculosis, biological control
Abbreviations: COSY, correlated spectroscopy
a The GenBank accession number for the sequence determined in this work is AY127079.
This article has been cited by other articles:
![]() |
S. Qin, J. Li, H.-H. Chen, G.-Z. Zhao, W.-Y. Zhu, C.-L. Jiang, L.-H. Xu, and W.-J. Li Isolation, Diversity, and Antimicrobial Activity of Rare Actinobacteria from Medicinal Plants of Tropical Rain Forests in Xishuangbanna, China Appl. Envir. Microbiol., October 1, 2009; 75(19): 6176 - 6186. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Compant, B. Duffy, J. Nowak, C. Clement, and E. A. Barka Use of Plant Growth-Promoting Bacteria for Biocontrol of Plant Diseases: Principles, Mechanisms of Action, and Future Prospects Appl. Envir. Microbiol., September 1, 2005; 71(9): 4951 - 4959. [Full Text] [PDF] |
||||
![]() |
D. Ezra, U. F. Castillo, G. A. Strobel, W. M. Hess, H. Porter, J. B. Jensen, M. A. M. Condron, D. B. Teplow, J. Sears, M. Maranta, et al. Coronamycins, peptide antibiotics produced by a verticillate Streptomyces sp. (MSU-2110) endophytic on Monstera sp. Microbiology, April 1, 2004; 150(4): 785 - 793. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Strobel and B. Daisy Bioprospecting for Microbial Endophytes and Their Natural Products Microbiol. Mol. Biol. Rev., December 1, 2003; 67(4): 491 - 502. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. L. Challis and D. A. Hopwood Synergy and contingency as driving forces for the evolution of multiple secondary metabolite production by Streptomyces species PNAS, November 25, 2003; 100(suppl_2): 14555 - 14561. [Abstract] [Full Text] |
||||
![]() |
From the Library Br J Ophthalmol, March 1, 2003; 87(3): 378 - 378. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |