Synthesis of bradyrhizose oligosaccharides relevant to the Bradyrhizobium O-antigen

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Standard

Synthesis of bradyrhizose oligosaccharides relevant to the Bradyrhizobium O-antigen. / Li, Wei; Silipo, Alba; Gersby, Lotte Bettina Andersen; Newman, Mari-Anne; Molinaro, Antonio; Yu, Biao.

I: Angewandte Chemie International Edition, Bind 56, Nr. 8, 2017, s. 2092-2096.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Li, W, Silipo, A, Gersby, LBA, Newman, M-A, Molinaro, A & Yu, B 2017, 'Synthesis of bradyrhizose oligosaccharides relevant to the Bradyrhizobium O-antigen', Angewandte Chemie International Edition, bind 56, nr. 8, s. 2092-2096. https://doi.org/10.1002/anie.201610680

APA

Li, W., Silipo, A., Gersby, L. B. A., Newman, M-A., Molinaro, A., & Yu, B. (2017). Synthesis of bradyrhizose oligosaccharides relevant to the Bradyrhizobium O-antigen. Angewandte Chemie International Edition, 56(8), 2092-2096. https://doi.org/10.1002/anie.201610680

Vancouver

Li W, Silipo A, Gersby LBA, Newman M-A, Molinaro A, Yu B. Synthesis of bradyrhizose oligosaccharides relevant to the Bradyrhizobium O-antigen. Angewandte Chemie International Edition. 2017;56(8):2092-2096. https://doi.org/10.1002/anie.201610680

Author

Li, Wei ; Silipo, Alba ; Gersby, Lotte Bettina Andersen ; Newman, Mari-Anne ; Molinaro, Antonio ; Yu, Biao. / Synthesis of bradyrhizose oligosaccharides relevant to the Bradyrhizobium O-antigen. I: Angewandte Chemie International Edition. 2017 ; Bind 56, Nr. 8. s. 2092-2096.

Bibtex

@article{612a702b28c54643a9eada14edd90c8d,

title = "Synthesis of bradyrhizose oligosaccharides relevant to the Bradyrhizobium O-antigen",

abstract = "The unique α-(1→7)-bradyrhizoside linkages are constructed for the first time via judicious choice of the glycosylation partners and conditions, thus tetra- and penta-bradyrhizosides relevant to the peculiar O-antigen of Bradyrhizobium are synthesized, which are shown to adopt the defined right-handed helical conformations and to be unable to induce innate immune responses in plants.",

keywords = "Journal Article",

author = "Wei Li and Alba Silipo and Gersby, {Lotte Bettina Andersen} and Mari-Anne Newman and Antonio Molinaro and Biao Yu",

note = "{\textcopyright} 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.",

year = "2017",

doi = "10.1002/anie.201610680",

language = "English",

volume = "56",

pages = "2092--2096",

journal = "Angewandte Chemie International Edition",

issn = "1433-7851",

publisher = "Wiley-VCH Verlag GmbH & Co. KGaA",

number = "8",

}

RIS

TY - JOUR

T1 - Synthesis of bradyrhizose oligosaccharides relevant to the Bradyrhizobium O-antigen

AU - Li, Wei

AU - Silipo, Alba

AU - Gersby, Lotte Bettina Andersen

AU - Newman, Mari-Anne

AU - Molinaro, Antonio

AU - Yu, Biao

PY - 2017

Y1 - 2017

N2 - The unique α-(1→7)-bradyrhizoside linkages are constructed for the first time via judicious choice of the glycosylation partners and conditions, thus tetra- and penta-bradyrhizosides relevant to the peculiar O-antigen of Bradyrhizobium are synthesized, which are shown to adopt the defined right-handed helical conformations and to be unable to induce innate immune responses in plants.

AB - The unique α-(1→7)-bradyrhizoside linkages are constructed for the first time via judicious choice of the glycosylation partners and conditions, thus tetra- and penta-bradyrhizosides relevant to the peculiar O-antigen of Bradyrhizobium are synthesized, which are shown to adopt the defined right-handed helical conformations and to be unable to induce innate immune responses in plants.

KW - Journal Article

U2 - 10.1002/anie.201610680

DO - 10.1002/anie.201610680

M3 - Journal article

C2 - 28097754

VL - 56

SP - 2092

EP - 2096

JO - Angewandte Chemie International Edition

JF - Angewandte Chemie International Edition

SN - 1433-7851

IS - 8

ER -

ID: 179928759