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Please use this identifier to cite or link to this item: http://scholars.ntou.edu.tw/handle/123456789/21316
Title: Lipopolysaccharide and beta-1,3-glucan-binding protein (LGBP) bind to seaweed polysaccharides and activate the prophenoloxidase system in white shrimp Litopenaeus vannamei
Authors: Yu-Yuan Chen
Jiann-Chu Chen 
Yi-Hsuan Kuo
Yong-Chin Lin
Yu-Hsuan Chang
Hong-Yi Gong 
Chien-Lun Huang
Keywords: CRAYFISH PACIFASTACUS-LENIUSCULUS;PATTERN-RECOGNITION PROTEIN;BLACK TIGER SHRIMP;HOT-WATER EXTRACT;MOLECULAR-CLONING;KURUMA SHRIMP;GRACILARIA-TENUISTIPITATA;PENAEUS-CALIFORNIENSIS;VIBRIO-ALGINOLYTICUS;DISEASE RESISTANCE
Issue Date: Feb-2016
Publisher: ELSEVIER
Journal Volume: 55
Start page/Pages: 144-151
Source: Developmental and Comparative Immunology
Abstract: 
Lipopolysaccharide and beta-1,3-glucan-binding protein (LGBP), important pattern recognition proteins (PRPs), recognize lipopolysaccharide (LPS) and beta-1,3-glucan (beta G), known as pathogen-associated molecular patterns (PAMPs), and subsequently trigger innate immunity. Several seaweed polysaccharides and seaweed extracts increase immune parameters and resistance to pathogens. Here, we constructed the expression vector pET28b-LvLGBP and transferred it into Escherichia coli BL21 (DE3) for protein expression and to produce the recombinant protein LGBP (rLAGBP) in white shrimp Litopenaeus vannamei. We examined the binding of rLvLGBP with seaweed-derived polysaccharides including alginate, carrageenan, fucoidan, laminarin, Gracilaria tenuisdpitata extract (GTE), and Sargassum duplicatum extract (SDE), and examined the phenoloxidase activity of shrimp haemocytes incubated with a mixture of rLvLGBP and each polysaccharide. We also examined the binding of rLvLGBP with EPS and beta G, and the phenoloxidase activity of shrimp haemocytes incubated with a mixture of rLvLGBP and LPS (rLvLGBP-LPS) or a mixture of rLvLGBP and beta G (rLvLGBP-beta G). An ELISA binding assay indicated that rLvLGBP binds to LPS, beta G, alginate, carrageenan, fucoidan, laminarin, GTE, and SDE with dissociation constants of 0.1138 -0.1770 mu M. Furthermore, our results also indicated that the phenoloxidase activity of shrimp haemocytes incubated with a mixture of rLvLGBP and LPS, beta G, alginate, carrageenan, fucoidan, laminarin, GTE, and SDE significantly increased by 328%, 172%, 200%, 213%, 197%, 194%, 191%, and 197%, respectively compared to controls (cacodylate buffer). We conclude that LA/LGBP functions as a PRP, recognizes and binds to LPS, beta G, alginate, carrageenan, fucoidan, laminarin, GTE, and SDE, and subsequently leads to activating innate immunity in shrimp. (C) 2015 Elsevier Ltd. All rights reserved.
URI: http://scholars.ntou.edu.tw/handle/123456789/21316
ISSN: 0145-305X
DOI: 10.1016/j.dci.2015.10.023
Appears in Collections:水產養殖學系

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