
Arul Jayaraman
· Executive Associate Dean of the Texas A&M University College of EngineeringTexas A&M University · Chemical Engineering
Active 1965–2025
About
Arul Jayaraman is an Executive Associate Dean of the Texas A&M University College of Engineering, a Professor in the Department of Chemical Engineering, and holds the Ray B. Nesbitt Endowed Chair. He is also an affiliated faculty member in Biomedical Engineering. His educational background includes a Ph.D. from the University of California, Irvine, obtained in 1998, an M.S. from Tufts University in 1994, and a B.S. from Birla Institute of Technology & Science in 1987. His research interests focus on molecular systems biotechnology, particularly on using integrated experimental and modeling approaches to investigate problems related to human health and medicine. His work encompasses systems biology of cytokine signaling in inflammatory diseases, inter-kingdom signaling interactions between bacteria and human cells in gastrointestinal tract infections, and the development of microfluidic model systems for combinatorial drug screening and vascular tissue engineering. Dr. Jayaraman has received numerous awards and honors, including being named a Texas A&M Presidential Impact Fellow in 2017, holding the Ray Nesbitt Chair since 2016, and being recognized as a Fellow of the American Institute of Medical and Biological Engineering in 2015. His contributions to the field are reflected in his leadership roles, research achievements, and recognition for teaching excellence.
Research topics
- Biochemistry
- Biology
- Chemistry
- Pharmacology
- Cell biology
- Medicine
- Cancer research
- Psychiatry
- Bioinformatics
- Endocrinology
- Computational biology
- Microbiology
- Internal medicine
Selected publications
Lab on a Chip · 2025-01-01 · 1 citations
articleOpen access1st authorCorrespondingmodels to study the role of microbial metabolism of dietary molecules on colorectal cancer colonocyte viability in the presence of macrophages.
Journal of Affective Disorders · 2022 · 17 citations
- Pharmacology
- Internal medicine
- Chemistry
Flavonoids: structure–function and mechanisms of action and opportunities for drug development
Toxicological Research · 2021 · 162 citations
- Pharmacology
- Computational biology
- Medicine
The EMBO Journal · 2020 · 43 citations
- Biology
- Cell biology
- Cancer research
Biphasic chemotaxis of <i>Escherichia coli</i> to the microbiota metabolite indole
Proceedings of the National Academy of Sciences · 2020 · 68 citations
- Microbiology
- Chemistry
- Biology
to a range of indole concentrations and measured the dynamic responses of individual flagellar motors to determine the chemotaxis response. Below 1 mM indole, a repellent-only response was observed. At 1 mM indole and higher, a time-dependent inversion from a repellent to an attractant response was observed. The repellent and attractant responses were mediated by the Tsr and Tar chemoreceptors, respectively. Also, the flagellar motor itself mediated a repellent response independent of the receptors. Chemotaxis assays revealed that receptor-mediated adaptation to indole caused a bipartite response-wild-type cells were attracted to regions of high indole concentration if they had previously adapted to indole but were otherwise repelled. We propose that indole spatially segregates cells based on their state of adaptation to repel invaders while recruiting beneficial resident bacteria to growing microbial communities within the GI tract.
Aryl Hydrocarbon Receptor (AHR) Ligands as Selective AHR Modulators (SAhRMs)
International Journal of Molecular Sciences · 2020 · 127 citations
Senior authorCorresponding- Chemistry
- Biochemistry
- Pharmacology
The aryl hydrocarbon receptor (AhR) was first identified as the intracellular protein that bound and mediated the toxic effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, dioxin) and dioxin-like compounds (DLCs). Subsequent studies show that the AhR plays an important role in maintaining cellular homeostasis and in pathophysiology, and there is increasing evidence that the AhR is an important drug target. The AhR binds structurally diverse compounds, including pharmaceuticals, phytochemicals and endogenous biochemicals, some of which may serve as endogenous ligands. Classification of DLCs and non-DLCs based on their persistence (metabolism), toxicities, binding to wild-type/mutant AhR and structural similarities have been reported. This review provides data suggesting that ligands for the AhR are selective AhR modulators (SAhRMs) that exhibit tissue/cell-specific AhR agonist and antagonist activities, and that their functional diversity is similar to selective receptor modulators that target steroid hormone and other nuclear receptors.
Recent grants
NIH · $380k · 2015
NSF · $1.1M · 2009–2013
Dietary Flavonoids-Microbiota-Ah Receptor Interactions in the Gut
NIH · $1.9M · 2018–2023
Diet induced modifications of microbiota metabolites in colon tumorigenesis
NIH · $2.0M · 2016–2021
CAREER: Inter-kingdom Signaling as a Paradigm for Molecular Systems Biology
NSF · $400k · 2009–2014
Frequent coauthors
- 116 shared
Robert C. Alaniz
Texas A&M Health Science Center
- 104 shared
Kyongbum Lee
Tufts University
- 98 shared
Martin L. Yarmush
Shriners Hospitals for Children - Boston
- 75 shared
Rani Menon
Texas A&M University
- 66 shared
Robert S. Chapkin
Texas A&M University
- 65 shared
Stephen Safe
Texas A&M University
- 56 shared
Evelyn Callaway
Texas A&M University
- 52 shared
Yufang Ding
Texas A&M University
Education
- 1998
PhD, Chemical Engineering
University of California, Irvine
- 1994
MS, Chemical and Biological Engineering
Tufts University
- 1992
B.E (Hons), Chemical Engineering
Birla Institute of Technology and Science
- 1992
M.Sc (Hons), Physics
Birla Institute of Technology and Science
Awards & honors
- Texas A&M Presidential Impact Fellow (2017)
- Texas Engineering Experiment Station Select Fellow (2017)
- Holder of the Ray Nesbitt Chair (2016)
- Fellow, American Institute of Medical and Biological Enginee…
- Engineering Genesis Award, Texas A&M Engineering Experiment…
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