Actinomycete Metabolome Induction/Suppression with N-Acetylglucosamine

被引:33
作者
Dashti, Yousef [1 ]
Grkovic, Tanja [1 ]
Abdelmohsen, Usama Ramadan [2 ,3 ]
Hentschel, Ute [2 ]
Quinn, Ronald J. [1 ]
机构
[1] Griffith Univ, Eskitis Inst Drug Discovery, Brisbane, Qld 4111, Australia
[2] Univ Wurzburg, Julius von Sachs Inst Biol Sci, Dept Bot 2, Julius von Sachs Pl 3, D-97082 Wurzburg, Germany
[3] Minia Univ, Fac Pharm, Dept Pharmacognosy, Menia 61519, Egypt
来源
JOURNAL OF NATURAL PRODUCTS | 2017年 / 80卷 / 04期
基金
澳大利亚研究理事会;
关键词
ELECTRONIC CIRCULAR-DICHROISM; NATURAL-PRODUCTS; GENOME SEQUENCE; SECONDARY METABOLITES; ANTIBIOTIC PRODUCTION; BACILLUS-SUBTILIS; DRUG DISCOVERY; SURFACTIN; ACID; BIOSYNTHESIS;
D O I
10.1021/acs.jnatprod.6b00673
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The metabolite profiles of three sponge-derived actinomycetes, namely, Micromonospora sp. RV43, Rhodococcus sp. RV157, and Actinokineospora sp. EG49 were investigated after elicitation with N-acetyl-D-glucosamine. H-1 NMR finger-print methodology was utilized to study the differences in the metabolic profiles of the bacterial extracts before and after elicitation. Our study found that the addition of N-acetyl-D-glucosamine modified the secondary metabolite profiles of the three investigated actinomycete isolates. N-Acetyl-D-glucosamine induced the production of 3-formylindole (11) and guaymasol (12) in Micromonospora sp. RV43, the siderophore bacillibactin 16, and surfactin antibiotic 17 in Rhodococcus sp. RV157 and increased the production of minor metabolites actinosporins E-H (21-24) in Actinokineospora sp. EG49. These results highlight the use of NMR fingerprinting to detect changes in metabolism following addition of N-acetyl-D-glucosamine. N-Acetyl-D-glucosamine was shown to have multiple effects including suppression of metabolites, induction of new metabolites, and increased production of minor compounds.
引用
收藏
页码:828 / 836
页数:9
相关论文
共 74 条
[41]   Drug Discovery and Natural Products: End of an Era or an Endless Frontier? [J].
Li, Jesse W. -H. ;
Vederas, John C. .
SCIENCE, 2009, 325 (5937) :161-165
[42]  
Lide D. R., 2000, CRC handbook of chemistry and physics
[43]   A new antibiotic kills pathogens without detectable resistance [J].
Ling, Losee L. ;
Schneider, Tanja ;
Peoples, Aaron J. ;
Spoering, Amy L. ;
Engels, Ina ;
Conlon, Brian P. ;
Mueller, Anna ;
Schaeberle, Till F. ;
Hughes, Dallas E. ;
Epstein, Slava ;
Jones, Michael ;
Lazarides, Linos ;
Steadman, Victoria A. ;
Cohen, Douglas R. ;
Felix, Cintia R. ;
Fetterman, K. Ashley ;
Millett, William P. ;
Nitti, Anthony G. ;
Zullo, Ashley M. ;
Chen, Chao ;
Lewis, Kim .
NATURE, 2015, 517 (7535) :455-+
[44]   The intracellular pathogen Rhodococcus equi produces a catecholate siderophore required for saprophytic growth [J].
Miranda-CasoLuengo, Raul ;
Prescott, John F. ;
Vazquez-Boland, Jose A. ;
Meijer, Wim G. .
JOURNAL OF BACTERIOLOGY, 2008, 190 (05) :1631-1637
[45]  
MORRISON JD, 1976, TETRAHEDRON LETT, P1773
[46]   The role of GlcNAc in formation and function of extracellular matrices [J].
Moussian, Bernard .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 2008, 149 (02) :215-226
[47]   Future potential for anti-infectives from bacteria - How to exploit biodiversity and genomic potential [J].
Mueller, Rolf ;
Wink, Joachim .
INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2014, 304 (01) :3-13
[48]   Environmental applications for biosurfactants [J].
Mulligan, CN .
ENVIRONMENTAL POLLUTION, 2005, 133 (02) :183-198
[49]  
Naseem Shamoon, 2012, Commun Integr Biol, V5, P156, DOI 10.4161/cib.19034
[50]   Genomic basis for natural product biosynthetic diversity in the actinomycetes [J].
Nett, Markus ;
Ikeda, Haruo ;
Moore, Bradley S. .
NATURAL PRODUCT REPORTS, 2009, 26 (11) :1362-1384