Author
Listed:
- Jun Wang
(Merck Research Laboratories)
- Stephen M. Soisson
(Merck Research Laboratories)
- Katherine Young
(Merck Research Laboratories)
- Wesley Shoop
(Merck Research Laboratories
DuPont Stine-Haskell Research Center
LL Silver Consulting)
- Srinivas Kodali
(Merck Research Laboratories)
- Andrew Galgoci
(Merck Research Laboratories)
- Ronald Painter
(Merck Research Laboratories)
- Gopalakrishnan Parthasarathy
(Merck Research Laboratories)
- Yui S. Tang
(Merck Research Laboratories)
- Richard Cummings
(Merck Research Laboratories)
- Sookhee Ha
(Merck Research Laboratories)
- Karen Dorso
(Merck Research Laboratories)
- Mary Motyl
(Merck Research Laboratories)
- Hiranthi Jayasuriya
(Merck Research Laboratories)
- John Ondeyka
(Merck Research Laboratories)
- Kithsiri Herath
(Merck Research Laboratories)
- Chaowei Zhang
(Merck Research Laboratories)
- Lorraine Hernandez
(Merck Research Laboratories)
- John Allocco
(Merck Research Laboratories)
- Ángela Basilio
(Merck Research Laboratories)
- José R. Tormo
(Merck Research Laboratories)
- Olga Genilloud
(Merck Research Laboratories)
- Francisca Vicente
(Merck Research Laboratories)
- Fernando Pelaez
(Merck Research Laboratories)
- Lawrence Colwell
(Merck Research Laboratories)
- Sang Ho Lee
(Merck Research Laboratories)
- Bruce Michael
(Merck Research Laboratories)
- Thomas Felcetto
(Merck Research Laboratories)
- Charles Gill
(Merck Research Laboratories)
- Lynn L. Silver
(Merck Research Laboratories
DuPont Stine-Haskell Research Center
LL Silver Consulting)
- Jeffery D. Hermes
(Merck Research Laboratories)
- Ken Bartizal
(Merck Research Laboratories)
- John Barrett
(Merck Research Laboratories)
- Dennis Schmatz
(Merck Research Laboratories)
- Joseph W. Becker
(Merck Research Laboratories)
- Doris Cully
(Merck Research Laboratories)
- Sheo B. Singh
(Merck Research Laboratories)
Abstract
New-wave antibiotics The worldwide spread of antibiotic resistance in pathogenic bacteria raises serious concerns that today's front-line antibiotics may become ineffective. So the discovery of a new class of compound with enormous potential as antibiotics is of great interest. Platensimycin is the first member of a novel class of natural products that selectively kills bacteria by inhibiting FabF/FabB proteins, a mechanism of action that is not used by any agents in clinical use. It is a potent antibiotic with broad-spectrum activity against Gram-positive bacteria, including clinically relevant drug-resistant bacteria, such as methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococcus. The future of platensimycins is considered in the News pages, and see the antimicrobials Web Focus on http://tinyurl.com/g8omx.
Suggested Citation
Jun Wang & Stephen M. Soisson & Katherine Young & Wesley Shoop & Srinivas Kodali & Andrew Galgoci & Ronald Painter & Gopalakrishnan Parthasarathy & Yui S. Tang & Richard Cummings & Sookhee Ha & Karen , 2006.
"Platensimycin is a selective FabF inhibitor with potent antibiotic properties,"
Nature, Nature, vol. 441(7091), pages 358-361, May.
Handle:
RePEc:nat:nature:v:441:y:2006:i:7091:d:10.1038_nature04784
DOI: 10.1038/nature04784
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Cited by:
- Katherine A. Ray & Joshua D. Lutgens & Ramesh Bista & Jie Zhang & Ronak R. Desai & Melissa Hirsch & Takeshi Miyazawa & Antonio Cordova & Adrian T. Keatinge-Clay, 2024.
"Assessing and harnessing updated polyketide synthase modules through combinatorial engineering,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
- Clara Lambert & Marine Gaillard & Paprapach Wongdontree & Caroline Bachmann & Antoine Hautcoeur & Karine Gloux & Thomas Guilbert & Celine Méhats & Bastien Prost & Audrey Solgadi & Sonia Abreu & Muriel, 2024.
"The double-edged role of FASII regulator FabT in Streptococcus pyogenes infection,"
Nature Communications, Nature, vol. 15(1), pages 1-14, December.
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