-
Something wrong with this record ?
Engineered Glycosidases for the Synthesis of Analogs of Human Milk Oligosaccharides
P. Nekvasilová, M. Hovorková, Z. Mészáros, L. Petrásková, H. Pelantová, V. Křen, K. Slámová, P. Bojarová
Language English Country Switzerland
Document type Journal Article
Grant support
20-00215S
Czech Science Foundation
LTC20072
Ministry of Education Youth and Sports
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
35456924
DOI
10.3390/ijms23084106
Knihovny.cz E-resources
- MeSH
- Bifidobacterium bifidum * metabolism MeSH
- Glycoside Hydrolases metabolism MeSH
- Glycosyltransferases metabolism MeSH
- Humans MeSH
- Milk, Human * metabolism MeSH
- Infant, Newborn MeSH
- Oligosaccharides chemistry MeSH
- Substrate Specificity MeSH
- Check Tag
- Humans MeSH
- Infant, Newborn MeSH
- Publication type
- Journal Article MeSH
Enzymatic synthesis is an elegant biocompatible approach to complex compounds such as human milk oligosaccharides (HMOs). These compounds are vital for healthy neonatal development with a positive impact on the immune system. Although HMOs may be prepared by glycosyltransferases, this pathway is often complicated by the high price of sugar nucleotides, stringent substrate specificity, and low enzyme stability. Engineered glycosidases (EC 3.2.1) represent a good synthetic alternative, especially if variations in the substrate structure are desired. Site-directed mutagenesis can improve the synthetic process with higher yields and/or increased reaction selectivity. So far, the synthesis of human milk oligosaccharides by glycosidases has mostly been limited to analytical reactions with mass spectrometry detection. The present work reveals the potential of a library of engineered glycosidases in the preparative synthesis of three tetrasaccharides derived from lacto-N-tetraose (Galβ4GlcNAcβ3Galβ4Glc), employing sequential cascade reactions catalyzed by β3-N-acetylhexosaminidase BbhI from Bifidobacterium bifidum, β4-galactosidase BgaD-B from Bacillus circulans, β4-N-acetylgalactosaminidase from Talaromyces flavus, and β3-galactosynthase BgaC from B. circulans. The reaction products were isolated and structurally characterized. This work expands the insight into the multi-step catalysis by glycosidases and shows the path to modified derivatives of complex carbohydrates that cannot be prepared by standard glycosyltransferase methods.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22018840
- 003
- CZ-PrNML
- 005
- 20220804135132.0
- 007
- ta
- 008
- 220720s2022 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/ijms23084106 $2 doi
- 035 __
- $a (PubMed)35456924
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Nekvasilová, Pavlína $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, CZ-14220 Praha, Czech Republic $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Viničná 5, CZ-12843 Praha, Czech Republic
- 245 10
- $a Engineered Glycosidases for the Synthesis of Analogs of Human Milk Oligosaccharides / $c P. Nekvasilová, M. Hovorková, Z. Mészáros, L. Petrásková, H. Pelantová, V. Křen, K. Slámová, P. Bojarová
- 520 9_
- $a Enzymatic synthesis is an elegant biocompatible approach to complex compounds such as human milk oligosaccharides (HMOs). These compounds are vital for healthy neonatal development with a positive impact on the immune system. Although HMOs may be prepared by glycosyltransferases, this pathway is often complicated by the high price of sugar nucleotides, stringent substrate specificity, and low enzyme stability. Engineered glycosidases (EC 3.2.1) represent a good synthetic alternative, especially if variations in the substrate structure are desired. Site-directed mutagenesis can improve the synthetic process with higher yields and/or increased reaction selectivity. So far, the synthesis of human milk oligosaccharides by glycosidases has mostly been limited to analytical reactions with mass spectrometry detection. The present work reveals the potential of a library of engineered glycosidases in the preparative synthesis of three tetrasaccharides derived from lacto-N-tetraose (Galβ4GlcNAcβ3Galβ4Glc), employing sequential cascade reactions catalyzed by β3-N-acetylhexosaminidase BbhI from Bifidobacterium bifidum, β4-galactosidase BgaD-B from Bacillus circulans, β4-N-acetylgalactosaminidase from Talaromyces flavus, and β3-galactosynthase BgaC from B. circulans. The reaction products were isolated and structurally characterized. This work expands the insight into the multi-step catalysis by glycosidases and shows the path to modified derivatives of complex carbohydrates that cannot be prepared by standard glycosyltransferase methods.
- 650 12
- $a Bifidobacterium bifidum $x metabolismus $7 D000069985
- 650 _2
- $a glykosidhydrolasy $x metabolismus $7 D006026
- 650 _2
- $a glykosyltransferasy $x metabolismus $7 D016695
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a novorozenec $7 D007231
- 650 12
- $a mateřské mléko $x metabolismus $7 D008895
- 650 _2
- $a oligosacharidy $x chemie $7 D009844
- 650 _2
- $a substrátová specifita $7 D013379
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Hovorková, Michaela $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, CZ-14220 Praha, Czech Republic $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Viničná 5, CZ-12843 Praha, Czech Republic
- 700 1_
- $a Mészáros, Zuzana $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, CZ-14220 Praha, Czech Republic $u Faculty of Food and Biochemical Technology, University of Chemistry and Technology Prague, Technická 1903/3, CZ-16628 Praha, Czech Republic $1 https://orcid.org/000000030137092X
- 700 1_
- $a Petrásková, Lucie $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, CZ-14220 Praha, Czech Republic $1 https://orcid.org/0000000270525115 $7 xx0101789
- 700 1_
- $a Pelantová, Helena $u Laboratory of Molecular Structure Characterization, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, CZ-14220 Praha, Czech Republic $1 https://orcid.org/0000000225237413
- 700 1_
- $a Křen, Vladimír $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, CZ-14220 Praha, Czech Republic $1 https://orcid.org/0000000210914020 $7 xx0070803
- 700 1_
- $a Slámová, Kristýna $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, CZ-14220 Praha, Czech Republic $1 https://orcid.org/0000000177727900 $7 xx0125284
- 700 1_
- $a Bojarová, Pavla $u Laboratory of Biotransformation, Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, CZ-14220 Praha, Czech Republic $1 https://orcid.org/0000000170690973 $7 xx0122667
- 773 0_
- $w MED00176142 $t International journal of molecular sciences $x 1422-0067 $g Roč. 23, č. 8 (2022)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/35456924 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220720 $b ABA008
- 991 __
- $a 20220804135126 $b ABA008
- 999 __
- $a ok $b bmc $g 1822440 $s 1170083
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2022 $b 23 $c 8 $e 20220407 $i 1422-0067 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
- GRA __
- $a 20-00215S $p Czech Science Foundation
- GRA __
- $a LTC20072 $p Ministry of Education Youth and Sports
- LZP __
- $a Pubmed-20220720