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Difference between revisions of "User:Nicole Koropatkin"

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[[Image: Nicole_Dec2016_small.jpg|thumb|widthpx| ]]Nicole Koropatkin received her PhD in Biochemistry from the University of Wisconsin in 2004. Trained in structural enzymology in the lab of Hazel Holden, her graduate work focused on the enymes involved in O-antigen deoxysugar biosynthesis in Salmonella typhi. After finishing her training, she moved to the lab of Thomas Smith at the Donald Danforth Plant Science Center in St. Louis. She received an NRSA to determine the structural basis for nitrate and bicarbonate discrimination within the ABC transport systems of Synechocystis PCC 6803.  After completing this study, she teamed up with Eric Martens from the Jeffrey Gordon lab at Washington University in St. Louis in order to investigate the structures of the novel proteins encoded within Bacteroidetes polysaccharide utilization loci. In 2009 she moved to the University of Michigan Medical School. She is currently an Assistant Professor in the Microbiology and Immunology department. The Koropatkin lab studies the structural biology of glycan capture by a variety of human gut bacteria.
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[[File:Nicole_Dec2016_small.jpg|200px|right]]Nicole Koropatkin received her PhD in Biochemistry from the University of Wisconsin in 2004. Trained in structural enzymology in the lab of Hazel Holden, her graduate work focused on the enymes involved in O-antigen deoxysugar biosynthesis in Salmonella typhi. After finishing her training, she moved to the lab of Thomas Smith at the Donald Danforth Plant Science Center in St. Louis. She received an NRSA to determine the structural basis for nitrate and bicarbonate discrimination within the ABC transport systems of Synechocystis PCC 6803.  After completing this study, she teamed up with Eric Martens from the Jeffrey Gordon lab at Washington University in St. Louis in order to investigate the structures of the novel proteins encoded within Bacteroidetes polysaccharide utilization loci. In 2009 she moved to the [https://www.umms.med.umich.edu/pibsfacsearch/facultyPage.do?facUniqname=nkoropat University of Michigan Medical School]. She is currently an [https://medicine.umich.edu/dept/microbiology-immunology/nicole-m-koropatkin-phd Assistant Professor in the Microbiology and Immunology department]. The Koropatkin lab studies the structural biology of glycan capture by a variety of human gut bacteria.
  
  
== References ==
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== Selected Citations ==
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<biblio>
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#Koropatkin2009 pmid=18611383
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#Martens2009 pmid=19553672
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#Koropatkin2010 pmid=20159465
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#Cameron2014 pmid=25205092
  
<references />
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#Karunatilaka2014 pmid=25389179
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#Cockburn2015 pmid=25388295
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#Foley2016 pmid=27137179
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#Tauzin2016 pmid=27118585
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#Larsbrink2016 pmid=27933102
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#Cockburn2016 pmid=27393306
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#Wefers2017 pmid=28669823
 +
 
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</biblio>
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<!--- Note: Do not remove this Category tag --->
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[[Category:Contributors|Koropatkin, Nicole]]

Latest revision as of 08:19, 6 September 2017

Nicole Dec2016 small.jpg

Nicole Koropatkin received her PhD in Biochemistry from the University of Wisconsin in 2004. Trained in structural enzymology in the lab of Hazel Holden, her graduate work focused on the enymes involved in O-antigen deoxysugar biosynthesis in Salmonella typhi. After finishing her training, she moved to the lab of Thomas Smith at the Donald Danforth Plant Science Center in St. Louis. She received an NRSA to determine the structural basis for nitrate and bicarbonate discrimination within the ABC transport systems of Synechocystis PCC 6803. After completing this study, she teamed up with Eric Martens from the Jeffrey Gordon lab at Washington University in St. Louis in order to investigate the structures of the novel proteins encoded within Bacteroidetes polysaccharide utilization loci. In 2009 she moved to the University of Michigan Medical School. She is currently an Assistant Professor in the Microbiology and Immunology department. The Koropatkin lab studies the structural biology of glycan capture by a variety of human gut bacteria.


Selected Citations

Error fetching PMID 20159465:
Error fetching PMID 25205092:
Error fetching PMID 25389179:
Error fetching PMID 25388295:
Error fetching PMID 27137179:
Error fetching PMID 27118585:
Error fetching PMID 27393306:
Error fetching PMID 28669823:
  1. Koropatkin NM, Martens EC, Gordon JI, and Smith TJ. (2008). Starch catabolism by a prominent human gut symbiont is directed by the recognition of amylose helices. Structure. 2008;16(7):1105-15. DOI:10.1016/j.str.2008.03.017 | PubMed ID:18611383 [Koropatkin2009]
  2. Martens EC, Koropatkin NM, Smith TJ, and Gordon JI. (2009). Complex glycan catabolism by the human gut microbiota: the Bacteroidetes Sus-like paradigm. J Biol Chem. 2009;284(37):24673-7. DOI:10.1074/jbc.R109.022848 | PubMed ID:19553672 [Martens2009]
  3. Error fetching PMID 20159465: [Koropatkin2010]
  4. Error fetching PMID 25205092: [Cameron2014]
  5. Error fetching PMID 25389179: [Karunatilaka2014]
  6. Error fetching PMID 25388295: [Cockburn2015]
  7. Error fetching PMID 27137179: [Foley2016]
  8. Error fetching PMID 27118585: [Tauzin2016]
  9. Larsbrink J, Zhu Y, Kharade SS, Kwiatkowski KJ, Eijsink VG, Koropatkin NM, McBride MJ, and Pope PB. (2016). A polysaccharide utilization locus from Flavobacterium johnsoniae enables conversion of recalcitrant chitin. Biotechnol Biofuels. 2016;9:260. DOI:10.1186/s13068-016-0674-z | PubMed ID:27933102 [Larsbrink2016]
  10. Error fetching PMID 27393306: [Cockburn2016]
  11. Error fetching PMID 28669823: [Wefers2017]

All Medline abstracts: PubMed