User:Aditya M. Kunjapur: Difference between revisions

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''Ph.D. Candidate, Prather Lab''
''Post-doctoral research associate, Church Lab''


[[Image:Formal_Portrait.JPG|thumb|right|Aditya M. Kunjapur]]
[[Image: Kunjapurv2.jpg|thumb|right|Aditya Kunjapur]]


Department of Genetics


Harvard Medical School


Department of Chemical Engineering
77 Avenue Louis Pasteur, NRB


Massachusetts Institute of Technology
Boston, MA 02115
 
77 Massachusetts Avenue, Room 66-425
 
Cambridge, MA 02139
   
   
[[Special:Emailuser/Aditya M. Kunjapur|Email me through OpenWetWare]]
[[Special:Emailuser/Aditya M. Kunjapur|Email me through OpenWetWare]]
[[Prather Lab]], OWW
[http://web.mit.edu/prathergroup/ Prather Lab, MIT Website]


==Research interests==
==Research interests==
*Effect of protein scaffolding design on flux through a model pathway
*Microbial biofuel production


*Synthetic genome assembly
*Genome editing
*Sensor-based metabolic pathway optimization
*Microbial production of aldehydes


'''More Detailed Research Description:'''


Numerous applications of metabolic engineering may be able to benefit from the use of synthetic protein scaffold devices (Dueber et al., 2009; Moon et al., 2010). These scaffolds consist of protein domains that are designed to spatially recruit sequential pathway enzymes tagged with cognate peptide ligands. The resulting in vivo co-localization of these enzymes can increase pathway flux in E. coli.
==Education==
 
Conditions for pathways most likely to benefit from the use of scaffolding are unclear at this time. Similarly, the scaffolds are modular, and certain scaffold arrangements have performed better than others depending on the pathway (Whitaker and Dueber, 2011). The ability to correctly predict the scaffold architecture that will result in the greatest enhancement of pathway flux is eventually desired, particularly compared to the only current alternative of experimentally probing many permutations.
 
To facilitate understanding and adoption of these scaffolds for further metabolic engineering applications, my research focuses on using a model pathway to experimentally and computationally explore the effects of parameters such as scaffold arrangement and metabolite concentrations on the overall pathway flux. The selected pathway features enzymes exclusively with monomeric quaternary structure. Salient advantages of using this pathway are more predictable enzyme-scaffold complex structure and simpler kinetics than in either the mevalonate or glucaric acid pathways.
 
I am also examining whether protein scaffolds can be used to increase flux through one of the biofuel pathways under investigation in our lab.


References:
*2015 - Ph.D., Chemical Engineering, Massachusetts Institute of Technology
Dueber et al. Synthetic protein scaffolds provide modular control over metabolic flux. Nat. Biotech., 2009.
*2010 - B.S., Chemical Engineering, University of Texas at Austin
Moon et al. Use of modular, synthetic scaffolds for improved production of glucaric acid in engineering E. coli. Metab. Eng., 2010.
Whitaker and Dueber. Metabolic flux enhancement by synthetic protein scaffolding. Methods Enzymol., 2011.
 
==Education==
B.S. Chemical Engineering,


& Business Foundations Certification,


University of Texas at Austin, May 2010
==Publications==


==Work Experience==
https://scholar.google.com/citations?user=9u32ODcAAAAJ&hl=en&oi=ao
===Petroleum Industry===
*2010, 2009 - Summer Internships, Shell Oil Company
*2008 - Summer Internship, ExxonMobil Production Company
*2006, 2007 - Summer Internships, Shell Oil Company
===Teaching===
*2009 - Teaching Assistant, Material and Energy Balances, UT, (1 semester)
*2008, 2009 - Tutor, Transport Phenomena, UT (2 sems)
*2009 - Grader, Transport Phenomena, UT (1 sem)


==Useful Links==


<!-- ==Publications==-->
https://www.linkedin.com/pub/aditya-kunjapur/3a/5ba/231
<!-- Replace the PubMed ID's ("pmid=#######") below with the PubMed ID's for your publications. You can add or remove lines as needed -->


<!--==Useful links==-->
https://twitter.com/kunjapur

Latest revision as of 10:12, 27 April 2016

Post-doctoral research associate, Church Lab

Aditya Kunjapur

Department of Genetics

Harvard Medical School

77 Avenue Louis Pasteur, NRB

Boston, MA 02115

Email me through OpenWetWare

Research interests

  • Synthetic genome assembly
  • Genome editing
  • Sensor-based metabolic pathway optimization
  • Microbial production of aldehydes


Education

  • 2015 - Ph.D., Chemical Engineering, Massachusetts Institute of Technology
  • 2010 - B.S., Chemical Engineering, University of Texas at Austin


Publications

https://scholar.google.com/citations?user=9u32ODcAAAAJ&hl=en&oi=ao

Useful Links

https://www.linkedin.com/pub/aditya-kunjapur/3a/5ba/231

https://twitter.com/kunjapur