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Identification of a novel chitin-binding spore wall protein (NbSWP12) with a BAR-2 domain from Nosema bombycis (microsporidia)
by
MA, ZHENGANG
, WU, HAIJING
, PAN, GUOQING
, CHEN, JIE
, YANG, DONGLIN
, GENG, LINA
, LONG, MENGXIAN
, ZHOU, ZEYANG
, LI, TIAN
, MA, CHAO
, LI, ZHI
, LI, CHUNFENG
in
alkali treatment
/ Amino Acid Sequence
/ Cell Wall - chemistry
/ Cell Wall - metabolism
/ Chitin
/ Chitin - metabolism
/ Conserved Sequence
/ Electrophoresis, Gel, Two-Dimensional
/ fluorescent antibody technique
/ Fluorescent Antibody Technique, Indirect
/ Fungal Proteins - chemistry
/ Fungal Proteins - genetics
/ Fungal Proteins - metabolism
/ genes
/ Mass Spectrometry
/ Microsporidia
/ Nosema - chemistry
/ Nosema - cytology
/ Nosema - metabolism
/ Nosema bombycis
/ pathogenesis
/ phosphorylation
/ Phylogeny
/ Protein Binding
/ protein kinase C
/ Protein Structure, Tertiary
/ Sequence Alignment
/ sequence analysis
/ Sequence Analysis, DNA
/ Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
/ spores
/ Spores, Fungal
/ Transcription, Genetic
/ two-dimensional gel electrophoresis
2013
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Identification of a novel chitin-binding spore wall protein (NbSWP12) with a BAR-2 domain from Nosema bombycis (microsporidia)
by
MA, ZHENGANG
, WU, HAIJING
, PAN, GUOQING
, CHEN, JIE
, YANG, DONGLIN
, GENG, LINA
, LONG, MENGXIAN
, ZHOU, ZEYANG
, LI, TIAN
, MA, CHAO
, LI, ZHI
, LI, CHUNFENG
in
alkali treatment
/ Amino Acid Sequence
/ Cell Wall - chemistry
/ Cell Wall - metabolism
/ Chitin
/ Chitin - metabolism
/ Conserved Sequence
/ Electrophoresis, Gel, Two-Dimensional
/ fluorescent antibody technique
/ Fluorescent Antibody Technique, Indirect
/ Fungal Proteins - chemistry
/ Fungal Proteins - genetics
/ Fungal Proteins - metabolism
/ genes
/ Mass Spectrometry
/ Microsporidia
/ Nosema - chemistry
/ Nosema - cytology
/ Nosema - metabolism
/ Nosema bombycis
/ pathogenesis
/ phosphorylation
/ Phylogeny
/ Protein Binding
/ protein kinase C
/ Protein Structure, Tertiary
/ Sequence Alignment
/ sequence analysis
/ Sequence Analysis, DNA
/ Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
/ spores
/ Spores, Fungal
/ Transcription, Genetic
/ two-dimensional gel electrophoresis
2013
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Identification of a novel chitin-binding spore wall protein (NbSWP12) with a BAR-2 domain from Nosema bombycis (microsporidia)
by
MA, ZHENGANG
, WU, HAIJING
, PAN, GUOQING
, CHEN, JIE
, YANG, DONGLIN
, GENG, LINA
, LONG, MENGXIAN
, ZHOU, ZEYANG
, LI, TIAN
, MA, CHAO
, LI, ZHI
, LI, CHUNFENG
in
alkali treatment
/ Amino Acid Sequence
/ Cell Wall - chemistry
/ Cell Wall - metabolism
/ Chitin
/ Chitin - metabolism
/ Conserved Sequence
/ Electrophoresis, Gel, Two-Dimensional
/ fluorescent antibody technique
/ Fluorescent Antibody Technique, Indirect
/ Fungal Proteins - chemistry
/ Fungal Proteins - genetics
/ Fungal Proteins - metabolism
/ genes
/ Mass Spectrometry
/ Microsporidia
/ Nosema - chemistry
/ Nosema - cytology
/ Nosema - metabolism
/ Nosema bombycis
/ pathogenesis
/ phosphorylation
/ Phylogeny
/ Protein Binding
/ protein kinase C
/ Protein Structure, Tertiary
/ Sequence Alignment
/ sequence analysis
/ Sequence Analysis, DNA
/ Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
/ spores
/ Spores, Fungal
/ Transcription, Genetic
/ two-dimensional gel electrophoresis
2013
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Identification of a novel chitin-binding spore wall protein (NbSWP12) with a BAR-2 domain from Nosema bombycis (microsporidia)
Journal Article
Identification of a novel chitin-binding spore wall protein (NbSWP12) with a BAR-2 domain from Nosema bombycis (microsporidia)
2013
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Overview
The spore wall of Nosema bombycis plays an important role in microsporidian pathogenesis. Protein fractions from germinated spore coats were analysed by two-dimensional polyacrylamide gel electrophoresis and MALDI-TOF/TOF mass spectrometry. Three protein spots were identified as the hypothetical spore wall protein NbHSWP12. A BAR-2 domain (e-value: 1.35e-03) was identified in the protein, and an N-terminal protein-heparin interaction motif, a potential N-glycosylation site, and 16 phosphorylation sites primarily activated by protein kinase C were also predicted. The sequence analysis suggested that Nbhswp12 and its homologous genes are widely distributed among microsporidia. Additionally, Nbhswp12 gene homologues share similar sequence features. An indirect immunofluorescence analysis showed that NbHSWP12 localized to the spore wall, and thus we renamed it spore wall protein 12 (NbSWP12). Moreover, NbSWP12 could adhere to deproteinized N. bombycis chitin coats that were obtained by hot alkaline treatment. This novel N. bombycis spore wall protein may function in a structural capacity to facilitate microsporidial spore maintenance.
Publisher
Cambridge University Press
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