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Difference between revisions of "User:Johan Larsbrink"
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[[Image:JLarsbrink.jpg|thumb|200px|right]] | [[Image:JLarsbrink.jpg|thumb|200px|right]] | ||
| − | ''' | + | '''Associate Professor''' at the Department of Biology and Biological Engineering, [http://www.chalmers.se Chalmers University of Technology]. |
== 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 | + | 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. |
| − | 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</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>. |
== Selected papers == | == Selected papers == | ||
| Line 18: | Line 18: | ||
#Larsbrink2016 pmid=27933102 | #Larsbrink2016 pmid=27933102 | ||
#JAB2018 pmid=30083226 | #JAB2018 pmid=30083226 | ||
| + | #JAB2019 pmid=30814248 | ||
</biblio> | </biblio> | ||
Revision as of 06:19, 26 August 2019
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
- 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 |
- 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 |
- 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 |
- 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 |
- 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 |
- 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 |
- 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 |