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Difference between revisions of "User:Johan Larsbrink"

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== Background ==
 
== Background ==
  
I obtained a MSc degree in Biotechnology at the [http://www.kth.se Royal Institute of Technology (KTH)] in 2007, where I later also completed my PhD thesis under the supervision of ^^^Harry Brumer^^^, focusing on xyloglucan degradation <cite>Larsbrink2011 Larsbrink2014a Larsbrink2014b</cite>. After my PhD I worked as a postdoctoral fellow with Phil Pope and ^^^Vincent Eijsink^^^ at the [http://www.nmbu.no Norwegian University of Life Sciences (NMBU)], mainly on chitin degradation <cite>Larsbrink2016</cite>. In 2015 I was appointed Assistant Professor at Chalmers University of Technology, and in 2019 I was promoted to Associate Professor. My research focuses primarily on enzyme (CAZyme) discovery coupled to structural and biochemical characterization.
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I obtained a MSc degree in Biotechnology at the [http://www.kth.se Royal Institute of Technology (KTH)] in 2007, where I later also completed my PhD thesis under the supervision of [[User:Harry Brumer|Harry Brumer]], focusing on xyloglucan degradation <cite>Larsbrink2011 Larsbrink2014a Larsbrink2014b</cite>. After my PhD I worked as a postdoctoral fellow with Phil Pope and [[User:Vincent Eijsink|Vincent Eijsink]] at the [http://www.nmbu.no Norwegian University of Life Sciences (NMBU)], mainly on chitin degradation <cite>Larsbrink2016</cite>. In 2015 I was appointed Assistant Professor at Chalmers University of Technology, and in 2019 I was promoted to Associate Professor. My research focuses primarily on enzyme (CAZyme) discovery coupled to structural and biochemical characterization.
  
 
I have contributed to structure-function studies of CAZymes from various families, including [[GH5]] <cite>Larsbrink2014a</cite>, [[GH18]], [[GH31]] <cite>Larsbrink2011 Larsbrink2012 Larsbrink2014a</cite>, [[GH35]] <cite>Larsbrink2014b</cite>, and [[CE15]] <cite>JAB2018 JAB2019</cite>.
 
I have contributed to structure-function studies of CAZymes from various families, including [[GH5]] <cite>Larsbrink2014a</cite>, [[GH18]], [[GH31]] <cite>Larsbrink2011 Larsbrink2012 Larsbrink2014a</cite>, [[GH35]] <cite>Larsbrink2014b</cite>, and [[CE15]] <cite>JAB2018 JAB2019</cite>.

Revision as of 13:35, 18 December 2021

JLarsbrink.jpg

Associate Professor at the Department of Biology and Biological Engineering, Chalmers University of Technology.

Background

I obtained a MSc degree in Biotechnology at the Royal Institute of Technology (KTH) in 2007, where I later also completed my PhD thesis under the supervision of Harry Brumer, focusing on xyloglucan degradation [1, 2, 3]. After my PhD I worked as a postdoctoral fellow with Phil Pope and Vincent Eijsink at the Norwegian University of Life Sciences (NMBU), mainly on chitin degradation [4]. In 2015 I was appointed Assistant Professor at Chalmers University of Technology, and in 2019 I was promoted to Associate Professor. My research focuses primarily on enzyme (CAZyme) discovery coupled to structural and biochemical characterization.

I have contributed to structure-function studies of CAZymes from various families, including GH5 [2], GH18, GH31 [1, 2, 5], GH35 [3], and CE15 [6, 7].

Selected papers

  1. Larsbrink J, Izumi A, Ibatullin FM, Nakhai A, Gilbert HJ, Davies GJ, and Brumer H. (2011). Structural and enzymatic characterization of a glycoside hydrolase family 31 α-xylosidase from Cellvibrio japonicus involved in xyloglucan saccharification. Biochem J. 2011;436(3):567-80. DOI:10.1042/BJ20110299 | PubMed ID:21426303 [Larsbrink2011]
  2. Larsbrink J, Rogers TE, Hemsworth GR, McKee LS, Tauzin AS, Spadiut O, Klinter S, Pudlo NA, Urs K, Koropatkin NM, Creagh AL, Haynes CA, Kelly AG, Cederholm SN, Davies GJ, Martens EC, and Brumer H. (2014). A discrete genetic locus confers xyloglucan metabolism in select human gut Bacteroidetes. Nature. 2014;506(7489):498-502. DOI:10.1038/nature12907 | PubMed ID:24463512 [Larsbrink2014a]
  3. Larsbrink J, Thompson AJ, Lundqvist M, Gardner JG, Davies GJ, and Brumer H. (2014). A complex gene locus enables xyloglucan utilization in the model saprophyte Cellvibrio japonicus. Mol Microbiol. 2014;94(2):418-33. DOI:10.1111/mmi.12776 | PubMed ID:25171165 [Larsbrink2014b]
  4. 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]
  5. Larsbrink J, Izumi A, Hemsworth GR, Davies GJ, and Brumer H. (2012). Structural enzymology of Cellvibrio japonicus Agd31B protein reveals α-transglucosylase activity in glycoside hydrolase family 31. J Biol Chem. 2012;287(52):43288-99. DOI:10.1074/jbc.M112.416511 | PubMed ID:23132856 [Larsbrink2012]
  6. Arnling Bååth J, Mazurkewich S, Knudsen RM, Poulsen JN, Olsson L, Lo Leggio L, and Larsbrink J. (2018). Biochemical and structural features of diverse bacterial glucuronoyl esterases facilitating recalcitrant biomass conversion. Biotechnol Biofuels. 2018;11:213. DOI:10.1186/s13068-018-1213-x | PubMed ID:30083226 [JAB2018]
  7. Arnling Bååth J, Mazurkewich S, Poulsen JN, Olsson L, Lo Leggio L, and Larsbrink J. (2019). Structure-function analyses reveal that a glucuronoyl esterase from Teredinibacter turnerae interacts with carbohydrates and aromatic compounds. J Biol Chem. 2019;294(16):6635-6644. DOI:10.1074/jbc.RA119.007831 | PubMed ID:30814248 [JAB2019]

All Medline abstracts: PubMed