Identification and characterisation of the major allergen of Chinese mitten crab ( Eriocheir sinensis)

Tropomyosin (TM) from Chinese mitten crab ( Eriocheir sinensis) was purified to homogeneity and TM genes were amplified from three species of crab (Chinese mitten crab, mud crab and swimming crab), respectively. Sequence analysis showed that all three cloned DNA fragments had open reading frames of...

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Published inFood chemistry Vol. 111; no. 4; pp. 998 - 1003
Main Authors Liang, Yin-Long, Cao, Min-Jie, Su, Wen-Jin, Zhang, Ling-Jing, Huang, Yuan-Yuan, Liu, Guang-Ming
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 15.12.2008
[Amsterdam]: Elsevier Science
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Abstract Tropomyosin (TM) from Chinese mitten crab ( Eriocheir sinensis) was purified to homogeneity and TM genes were amplified from three species of crab (Chinese mitten crab, mud crab and swimming crab), respectively. Sequence analysis showed that all three cloned DNA fragments had open reading frames of 855 bp, predicted to encode proteins with 284 amino acid residues. Sequence alignment revealed that the three tropomyosins share high homology to tropomyosins from other crustaceans. Chinese mitten crab TM gene was further recombined with the vector of pGEX-4T-3 and expressed in Escherichia coli JM109. The expressed protein revealed a band of about 62 kDa on SDS–PAGE, suggesting the successful expression of glutathione S-transferase–tropomyosin (GST–TM) fusion protein. Immunoblotting analysis using sera from subjects with crustacean allergy confirmed that the expressed fusion protein reacted positively with these sera, indicating tropomyosin is a major allergen of Chinese mitten crab.
AbstractList Tropomyosin (TM) from Chinese mitten crab (Eriocheir sinensis) was purified to homogeneity and TM genes were amplified from three species of crab (Chinese mitten crab, mud crab and swimming crab), respectively. Sequence analysis showed that all three cloned DNA fragments had open reading frames of 855 bp, predicted to encode proteins with 284 amino acid residues. Sequence alignment revealed that the three tropomyosins share high homology to tropomyosins from other crustaceans. Chinese mitten crab TM gene was further recombined with the vector of pGEX-4T-3 and expressed in Escherichia coli JM109. The expressed protein revealed a band of about 62 kDa on SDS-PAGE, suggesting the successful expression of glutathione S-transferase-tropomyosin (GST-TM) fusion protein. Immunoblotting analysis using sera from subjects with crustacean allergy confirmed that the expressed fusion protein reacted positively with these sera, indicating tropomyosin is a major allergen of Chinese mitten crab.
Tropomyosin (TM) from Chinese mitten crab ( Eriocheir sinensis) was purified to homogeneity and TM genes were amplified from three species of crab (Chinese mitten crab, mud crab and swimming crab), respectively. Sequence analysis showed that all three cloned DNA fragments had open reading frames of 855 bp, predicted to encode proteins with 284 amino acid residues. Sequence alignment revealed that the three tropomyosins share high homology to tropomyosins from other crustaceans. Chinese mitten crab TM gene was further recombined with the vector of pGEX-4T-3 and expressed in Escherichia coli JM109. The expressed protein revealed a band of about 62 kDa on SDS–PAGE, suggesting the successful expression of glutathione S-transferase–tropomyosin (GST–TM) fusion protein. Immunoblotting analysis using sera from subjects with crustacean allergy confirmed that the expressed fusion protein reacted positively with these sera, indicating tropomyosin is a major allergen of Chinese mitten crab.
Tropomyosin (TM) from Chinese mitten crab (Eriocheir sinensis) was purified to homogeneity and TM genes were amplified from three species of crab (Chinese mitten crab, mud crab and swimming crab), respectively. Sequence analysis showed that all three cloned DNA fragments had open reading frames of 855bp, predicted to encode proteins with 284 amino acid residues. Sequence alignment revealed that the three tropomyosins share high homology to tropomyosins from other crustaceans. Chinese mitten crab TM gene was further recombined with the vector of pGEX-4T-3 and expressed in Escherichia coli JM109. The expressed protein revealed a band of about 62kDa on SDS-PAGE, suggesting the successful expression of glutathione S-transferase-tropomyosin (GST-TM) fusion protein. Immunoblotting analysis using sera from subjects with crustacean allergy confirmed that the expressed fusion protein reacted positively with these sera, indicating tropomyosin is a major allergen of Chinese mitten crab.
Author Liu, Guang-Ming
Huang, Yuan-Yuan
Cao, Min-Jie
Liang, Yin-Long
Zhang, Ling-Jing
Su, Wen-Jin
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Issue 4
Keywords Tropomyosin
Expression
Eriocheir sinensis
Cloning
Homology
Identification
Allergen
Crustacea
Crab
Edible crustacean
Arthropoda
Brachyura
Decapoda
Eriocheir sinensis,Allergen,Tropomyosin,Identification,Cloning,Homology,Expression
Invertebrata
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Snippet Tropomyosin (TM) from Chinese mitten crab ( Eriocheir sinensis) was purified to homogeneity and TM genes were amplified from three species of crab (Chinese...
Tropomyosin (TM) from Chinese mitten crab (Eriocheir sinensis) was purified to homogeneity and TM genes were amplified from three species of crab (Chinese...
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SubjectTerms Allergen
allergens
Biological and medical sciences
Cloning
crabs
Crustacea
Decapoda
Eriocheir sinensis
Escherichia coli
Expression
Fish and seafood industries
food allergies
food analysis
food composition
Food industries
Fundamental and applied biological sciences. Psychology
General aspects
genes
Homology
Identification
Methods of analysis, processing and quality control, regulation, standards
molecular sequence data
mud crab
open reading frames
protein synthesis
seafoods
sequence analysis
swimming crab
Tropomyosin
tropomyosins
Title Identification and characterisation of the major allergen of Chinese mitten crab ( Eriocheir sinensis)
URI https://dx.doi.org/10.1016/j.foodchem.2008.05.023
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