Sequential One-Pot Multienzyme Chemoenzymatic Synthesis of Glycosphingolipid Glycans

被引:57
|
作者
Yu, Hai [1 ,2 ]
Li, Yanhong [1 ,2 ]
Zeng, Jie [2 ,3 ]
Thon, Vireak [2 ,4 ]
Nguyen, Dung M. [2 ,5 ]
Ly, Thao [2 ]
Kuang, Hui Yu [2 ,6 ]
Ngo, Alice [2 ]
Chen, Xi [2 ]
机构
[1] Glycohub Inc, 4070 Truxel Rd, Sacramento, CA 95834 USA
[2] Univ Calif Davis, Dept Chem, One Shields Ave, Davis, CA 95616 USA
[3] Henan Inst Sci & Technol, Sch Food Sci, Xinxiang 453003, Henan, Peoples R China
[4] US FDA, Lab Bacterial Polysaccharides, Bethesda, MD 20892 USA
[5] Univ Calif Davis, Ctr Neurosci, Davis, CA 95616 USA
[6] Touro Univ, Coll Pharm, Vallejo, CA 94592 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2016年 / 81卷 / 22期
基金
美国国家卫生研究院;
关键词
GLOBO-H HEXASACCHARIDE; SIALYL-LEWIS-X; N-GLYCOLYLNEURAMINIC ACID; ESCHERICHIA-COLI; MONOCLONAL-ANTIBODY; ENZYMATIC-SYNTHESIS; HUMAN-MELANOMA; CANCER VACCINES; CHOLERA-TOXIN; GANGLIOSIDE;
D O I
10.1021/acs.joc.6b01905
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Glycosphingolipids are a diverse family of biologically important glycolipids. In addition to variations on the lipid component, more than 300 glycosphingolipid glycans have been characterized. These glycans are directly involved in various molecular recognition events. Several naturally occurring sialic acid forms have been found in sialic acid-containing glycosphingolipids, namely gangliosides. However, ganglioside glycans containing less common sialic acid forms are currently not available. Herein, highly effective one-pot multienzyme (OPME) systems are used in sequential for high-yield and cost-effective production of glycosphingolipid glycans, including those containing different sialic acid forms such as N-acetylneuraminic acid (Neu5Ac), N-glycolylneuraminic acid (Neu5Gc), 2-keto-3-deoxy-D-glycero-D-galacto-nononic acid (Kdn), and 8-0-methyl-N-acetylneuraminic acid (Neu5Ac8OMe). A library of 64 structurally distinct glycosphingolipid glycans belonging to ganglio-series, lacto-/neolacto-series, and globo-/isoglobo-series glycosphingolipid glycans is constructed. These glycans are essential standards and invaluable probes for bioassays and biomedical studies.
引用
收藏
页码:10809 / 10824
页数:16
相关论文
共 50 条
  • [31] One-pot chemoenzymatic preparation of coenzyme A analogues
    Nazi, I
    Koteva, KP
    Wright, GD
    ANALYTICAL BIOCHEMISTRY, 2004, 324 (01) : 100 - 105
  • [32] CHEMOENZYMATIC SYNTHESIS OF A GLYCOSPHINGOLIPID
    GUILBERT, B
    KHAN, TH
    FLITSCH, SL
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1992, (20) : 1526 - 1527
  • [33] Highly Efficient One-Pot Multienzyme Cascades for the Stereoselective Synthesis of Natural Naphthalenones
    De, Arijit
    Saha, Nirmal
    Manna, Tanaya
    Singh, Vidya
    Husain, Syed Masood
    ACS CATALYSIS, 2022, 12 (19): : 12179 - 12185
  • [34] One-pot multi-enzyme chemoenzymatic synthesis of LacNAc and its derivatives
    Lau, Kam
    Thon, Vireak
    Huang, Ronald
    Chen, Xi
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2010, 239
  • [35] Chemoenzymatic one-pot synthesis of enantiopure L-arylalanines from arylaldehydes
    Paizs, C
    Katona, A
    Rétey, J
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2006, 2006 (05) : 1113 - 1116
  • [36] Chiral (R)- and (S)-allylic alcohols via a one-pot chemoenzymatic synthesis
    Sgalla, Simona
    Fabrizi, Giancarlo
    Cirilli, Roberto
    Macone, Alberto
    Bonamore, Alessandra
    Boffi, Alberto
    Cacchi, Sandro
    TETRAHEDRON-ASYMMETRY, 2007, 18 (23) : 2791 - 2796
  • [37] A chemoenzymatic method for simultaneous profiling N- and O-glycans on glycoproteins using one-pot format
    Ortega-Rodriguez, Uriel
    Bettinger, John Q.
    Zou, Guozhang
    Falkowski, Vincent M.
    Lehtimaki, Mari
    Matthews, Alicia M.
    Biel, Thomas G.
    Pritts, Jordan D.
    Wu, Wells W.
    Shen, Rong-Fong
    Agarabi, Cyrus
    Rao, V. Ashutosh
    Xie, Hang
    Ju, Tongzhong
    CELL REPORTS METHODS, 2024, 4 (08):
  • [38] Synthetic Utility of One-Pot Chemoenzymatic Reaction Sequences
    Doyon, Tyler J.
    Narayan, Alison R. H.
    SYNLETT, 2020, 31 (03) : 230 - 236
  • [39] One-Pot Chemoenzymatic Conversion of Alkynes to Chiral Amines
    Mathew, Sam
    Sagadevan, Arunachalam
    Renn, Dominik
    Rueping, Magnus
    ACS CATALYSIS, 2021, 11 (20): : 12565 - 12569
  • [40] ONE-POT SEQUENTIAL GLYCOSYLATION - A NEW METHOD FOR THE SYNTHESIS OF OLIGOSACCHARIDES
    YAMADA, H
    HARADA, T
    MIYAZAKI, H
    TAKAHASHI, T
    TETRAHEDRON LETTERS, 1994, 35 (23) : 3979 - 3982