Picture of Jon Clardy

Jon Clardy, Ph.D.

Christopher T. Walsh Professor of Biological Chemistry and Molecular Pharmacology

The laboratory focuses on biologically active small molecules, especially those from bacteria and fungi with an overall goal of understanding how small molecules control biological processes. 

Research:

The laboratory focuses on biologically active small molecules, especially those from bacteria and fungi with an overall goal of understanding how small molecules control biological processes.  Organizing themes include: 1) function-based discovery of microbially-produced small molecules and their roles in microbial symbioses , 2) function-based discovery of biologically active small molecules using high-throughput screening,  3) genome-based discovery of bacterially-produced small molecules. 

1.  We have focused on the small molecule exchanges that underlie multilateral symbioses involving bacteria, partly because they are widespread and poorly understood and partly because they lead to the discovery of new useful molecules in the biological context in which they evolved.  Current projects involve the bacterial symbionts of fungus-growing ants, members of the human gut microbiome linked to disease, and interactions between micro-algae and bacteria.

2.  We also continue to discover small molecules in a more medically relevant context: high-throughput screening for a variety of diseases.  In these projects we have focused on antibacterial, antifungal, and antiparasitic agents along with immunomodulators and anticancer agents. 

3.  It is now quite clear that well studied bacteria – the producers of drugs that are used on the ton scale, for example – are genetically capable of producing many more potentially useful small molecules.  The biosynthetic gene can be seen but the associated molecules have never been characterized.  Ways to access these cryptic metabolites is a current focus of the laboratory.

Address: 

Room C-643

240 Longwood Avenue

Boston, MA 02115

Publications View
Total synthesis of psammaplysenes A and B, naturally occurring inhibitors of FOXO1a nuclear export.
Authors: Authors: Georgiades SN, Clardy J.
Org Lett
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N-acyl derivatives of arginine and tryptophan isolated from environmental DNA expressed in Escherichia coli.
Authors: Authors: Brady SF, Clardy J.
Org Lett
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Bacterial printing press that regenerates its ink: contact-printing bacteria using hydrogel stamps.
Authors: Authors: Weibel DB, Lee A, Mayer M, Brady SF, Bruzewicz D, Yang J, Diluzio WR, Clardy J, Whitesides GM.
Langmuir
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The psammaplysenes, specific inhibitors of FOXO1a nuclear export.
Authors: Authors: Schroeder FC, Kau TR, Silver PA, Clardy J.
J Nat Prod
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Using genomics to deliver natural products from symbiotic bacteria.
Authors: Authors: Clardy J.
Genome Biol
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Lessons from natural molecules.
Authors: Authors: Clardy J, Walsh C.
Nature
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Long-chain N-acyltyrosine synthases from environmental DNA.
Authors: Authors: Brady SF, Chao CJ, Clardy J.
Appl Environ Microbiol
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Palmitoylputrescine, an antibiotic isolated from the heterologous expression of DNA extracted from bromeliad tank water.
Authors: Authors: Brady SF, Clardy J.
J Nat Prod
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Transglutaminase 5 is regulated by guanine-adenine nucleotides.
Authors: Authors: Candi E, Paradisi A, Terrinoni A, Pietroni V, Oddi S, Cadot B, Jogini V, Meiyappan M, Clardy J, Finazzi-Agro A, Melino G.
Biochem J
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Tyrosol is a quorum-sensing molecule in Candida albicans.
Authors: Authors: Chen H, Fujita M, Feng Q, Clardy J, Fink GR.
Proc Natl Acad Sci U S A
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