User:Erik Quandt: Difference between revisions

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//Generalized bacterial genome editing using mobile group II introns and Cre-lox.
//Generalized bacterial genome editing using mobile group II introns and Cre-lox.


#paper5 pmid=24379390


#Book1 isbn=9781400848065
//Recursive genomewide recombination and sequencing reveals a key refinement step in the evolution of a metabolic innovation in Escherichia coli.
 
 
#Book1 isbn=9780691149776
</biblio>
</biblio>



Revision as of 08:01, 1 January 2014

I am a new member of OpenWetWare!

Contact Info

Erik Quandt (an artistic interpretation)
  • Erik Quandt
  • UT Austin
  • Co-advised by George Georgiou and Andy Ellington
  • Institute for Cell and Molecular Biology
  • 2500 Speedway, MBB 3.312
  • Austin, TX 78712-1095
  • Email me through OpenWetWare

I work in the Your Lab at XYZ University. I learned about OpenWetWare from Use site for molecular biology protocols, and I've joined because Enrolled in CH391L/S12: Synthetic Biology at UT Austin, would like to edit course web page.

Education

  • 2014, PhD, University of Texas at Austin
  • 2005, BS Biology, University of Georgia

Research interests

  1. Metagenomics
  2. Genome Engineering
  3. Strain Improvement

Publications

  1. Patrick WM, Quandt EM, Swartzlander DB, and Matsumura I. Multicopy suppression underpins metabolic evolvability. Mol Biol Evol. 2007 Dec;24(12):2716-22. DOI:10.1093/molbev/msm204 | PubMed ID:17884825 | HubMed [Paper1]

    Multicopy suppression underpins metabolic evolvability.

  2. Quandt EM, Hammerling MJ, Summers RM, Otoupal PB, Slater B, Alnahhas RN, Dasgupta A, Bachman JL, Subramanian MV, and Barrick JE. Decaffeination and measurement of caffeine content by addicted Escherichia coli with a refactored N-demethylation operon from Pseudomonas putida CBB5. ACS Synth Biol. 2013 Jun 21;2(6):301-7. DOI:10.1021/sb4000146 | PubMed ID:23654268 | HubMed [Paper2]

    Decaffeination and Measurement of Caffeine Content by Addicted Escherichia coli with a Refactored N-Demethylation Operon from Pseudomonas putida CBB5.

  3. Summers RM, Seffernick JL, Quandt EM, Yu CL, Barrick JE, and Subramanian MV. Caffeine junkie: an unprecedented glutathione S-transferase-dependent oxygenase required for caffeine degradation by Pseudomonas putida CBB5. J Bacteriol. 2013 Sep;195(17):3933-9. DOI:10.1128/JB.00585-13 | PubMed ID:23813729 | HubMed [Paper3]

    Caffeine junkie: an unprecedented glutathione S-transferase-dependent oxygenase required for caffeine degradation by Pseudomonas putida CBB5.

  4. Enyeart PJ, Chirieleison SM, Dao MN, Perutka J, Quandt EM, Yao J, Whitt JT, Keatinge-Clay AT, Lambowitz AM, and Ellington AD. Generalized bacterial genome editing using mobile group II introns and Cre-lox. Mol Syst Biol. 2013;9:685. DOI:10.1038/msb.2013.41 | PubMed ID:24002656 | HubMed [Paper4]

    Generalized bacterial genome editing using mobile group II introns and Cre-lox.

  5. Quandt EM, Deatherage DE, Ellington AD, Georgiou G, and Barrick JE. Recursive genomewide recombination and sequencing reveals a key refinement step in the evolution of a metabolic innovation in Escherichia coli. Proc Natl Acad Sci U S A. 2014 Feb 11;111(6):2217-22. DOI:10.1073/pnas.1314561111 | PubMed ID:24379390 | HubMed [paper5]

    Recursive genomewide recombination and sequencing reveals a key refinement step in the evolution of a metabolic innovation in Escherichia coli.

  6. ISBN:9780691149776 [Book1]

All Medline abstracts: PubMed | HubMed

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