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Difference between revisions of "User:Tomomi Sumida"

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Tomomi Sumida obtained her Ph.D. from the Department of Bioscience and Biotechnology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyusyu University, under the supervision of Professor Makoto Ito in 2010. She isolated the ganglioside–degrading bacterium ''Paenibacillus'' sp. strain TS12 from land soil in her doctoral research <cite>SumidaAEM2002</cite>. Strain TS12 produces a series of glycosphingolipid-degrading enzymes, such as sialidase, β-galactosidase, β-hexosaminidase, β-''N''-acetylgalactosaminidase, and β-glucocerebrosidase. She has reported the molecular cloning, characterization, and structural analysis of these novel glycosphingolipid-degrading enzymes, as follows:
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Tomomi Sumida obtained her Ph.D. from [http://www.agr.kyushu-u.ac.jp/english/ the Department of Bioscience and Biotechnology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyusyu University], under the supervision of Professor Makoto Ito in 2010. She isolated the ganglioside–degrading bacterium ''Paenibacillus'' sp. strain TS12 from land soil in her doctoral research <cite>SumidaAEM2002</cite>. Strain TS12 produces a series of glycosphingolipid-degrading enzymes, such as sialidase, β-galactosidase, β-hexosaminidase, β-''N''-acetylgalactosaminidase, and β-glucocerebrosidase. She has reported the molecular cloning, characterization, and structural analysis of these novel glycosphingolipid-degrading enzymes, as follows:
  
+
* [[GH3]] β-glucocerebrosidase (Glc4) from ''Paenibacillus'' sp. TS12 <cite>SumidaJB2002</cite>.
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* [[GH20]] β-hexosaminidase (Hex1) from ''Paenibacillus'' sp. TS12 <cite>SumidaJMB2009 SumidaOBC2012</cite>.
 +
* [[GH123]] β-''N''-acetylgalactosaminidase (NgaP) from ''Paenibacillus'' sp. TS12 <cite>SumidaJBC2011</cite>.
  
・GH3 β-glucocerebrosidase (Glc4) from ''Paenibacillus'' sp. TS12 <cite>SumidaJB2002</cite>.
+
NgaP, which specifically hydrolyzes the non-reducing terminal β-GalNAc linkage but not β-GlcNAc linkage, is the first β-''N''-acetylgalactosaminidase (EC 3.2.1.53) to have its primary structure elucidated. Since the primary structure of NgaP is totally new, [http://www.cazy.org/GH123.html GH123] was created as a new family of β-''N''-acetylgalactosaminidases in 2011.
  
・GH20 β-hexosaminidase (Hex1) from ''Paenibacillus'' sp. TS12 <cite>SumidaJMB2009</cite><cite>SumidaOBC2012</cite>.
 
  
・GH123 β-''N''-acetylgalactosaminidase (NgaP) from ''Paenibacillus'' sp. TS12 <cite>SumidaJBC2011</cite>.
 
 
 
 
NgaP, which specifically hydrolyzes the non-reducing terminal β-GalNAc linkage but not β-GlcNAc linkage, is the first β-''N''-acetylgalactosaminidase (EC 3.2.1.53) to have its primary structure elucidated. Since the primary structure of NgaP is totally new, class GH123 was created as a new family of β-''N''-acetylgalactosaminidase in 2011.
 
  
 
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<biblio>
 
<biblio>
 
 
#SumidaAEM2002 pmid=12406710
 
#SumidaAEM2002 pmid=12406710
 
</biblio>
 
 
<biblio>
 
 
 
#SumidaJB2002 pmid=12153721
 
#SumidaJB2002 pmid=12153721
 
</biblio>
 
 
<biblio>
 
 
 
#SumidaJMB2009 pmid=19524595
 
#SumidaJMB2009 pmid=19524595
 
</biblio>
 
 
<biblio>
 
 
 
#SumidaOBC2012 pmid=22367352
 
#SumidaOBC2012 pmid=22367352
 
</biblio>
 
 
<biblio>
 
 
 
#SumidaJBC2011 pmid=21297160
 
#SumidaJBC2011 pmid=21297160
  

Latest revision as of 02:39, 11 August 2016

Tomomi Sumida.jpg

Tomomi Sumida obtained her Ph.D. from the Department of Bioscience and Biotechnology, Graduate School of Bioresource and Bioenvironmental Sciences, Kyusyu University, under the supervision of Professor Makoto Ito in 2010. She isolated the ganglioside–degrading bacterium Paenibacillus sp. strain TS12 from land soil in her doctoral research [1]. Strain TS12 produces a series of glycosphingolipid-degrading enzymes, such as sialidase, β-galactosidase, β-hexosaminidase, β-N-acetylgalactosaminidase, and β-glucocerebrosidase. She has reported the molecular cloning, characterization, and structural analysis of these novel glycosphingolipid-degrading enzymes, as follows:

  • GH3 β-glucocerebrosidase (Glc4) from Paenibacillus sp. TS12 [2].
  • GH20 β-hexosaminidase (Hex1) from Paenibacillus sp. TS12 [3, 4].
  • GH123 β-N-acetylgalactosaminidase (NgaP) from Paenibacillus sp. TS12 [5].

NgaP, which specifically hydrolyzes the non-reducing terminal β-GalNAc linkage but not β-GlcNAc linkage, is the first β-N-acetylgalactosaminidase (EC 3.2.1.53) to have its primary structure elucidated. Since the primary structure of NgaP is totally new, GH123 was created as a new family of β-N-acetylgalactosaminidases in 2011.



  1. Sumida T, Sueyoshi N, and Ito M. (2002). Utilization of ganglioside-degrading Paenibacillus sp. strain TS12 for production of glucosylceramide. Appl Environ Microbiol. 2002;68(11):5241-8. DOI:10.1128/AEM.68.11.5241-5248.2002 | PubMed ID:12406710 [SumidaAEM2002]
  2. Sumida T, Sueyoshi N, and Ito M. (2002). Molecular cloning and characterization of a novel glucocerebrosidase of Paenibacillus sp. TS12. J Biochem. 2002;132(2):237-43. DOI:10.1093/oxfordjournals.jbchem.a003216 | PubMed ID:12153721 [SumidaJB2002]
  3. Sumida T, Ishii R, Yanagisawa T, Yokoyama S, and Ito M. (2009). Molecular cloning and crystal structural analysis of a novel beta-N-acetylhexosaminidase from Paenibacillus sp. TS12 capable of degrading glycosphingolipids. J Mol Biol. 2009;392(1):87-99. DOI:10.1016/j.jmb.2009.06.025 | PubMed ID:19524595 [SumidaJMB2009]
  4. Sumida T, Stubbs KA, Ito M, and Yokoyama S. (2012). Gaining insight into the inhibition of glycoside hydrolase family 20 exo-β-N-acetylhexosaminidases using a structural approach. Org Biomol Chem. 2012;10(13):2607-12. DOI:10.1039/c2ob06636j | PubMed ID:22367352 [SumidaOBC2012]
  5. Sumida T, Fujimoto K, and Ito M. (2011). Molecular cloning and catalytic mechanism of a novel glycosphingolipid-degrading beta-N-acetylgalactosaminidase from Paenibacillus sp. TS12. J Biol Chem. 2011;286(16):14065-72. DOI:10.1074/jbc.M110.182592 | PubMed ID:21297160 [SumidaJBC2011]

All Medline abstracts: PubMed