Cellulase degradation of shrimp chitosan for the preparation of a water-soluble hydrolysate with immunoactivity
Samples of colloidal chitin and chitosans with deacetylation degrees (DD) of 50, 65, 75 and 95% (DD5O, DD65, DD75 and DD95, respectively) were prepared from shrimp chitin. The hydrolytic activity of cellulase on these samples increased with the increasing DO of chitosan, with DD95 being the most eas...
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Veröffentlicht in: | Fisheries science 2004-12, Vol.70 (6), p.1113-1120 |
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description | Samples of colloidal chitin and chitosans with deacetylation degrees (DD) of 50, 65, 75 and 95% (DD5O, DD65, DD75 and DD95, respectively) were prepared from shrimp chitin. The hydrolytic activity of cellulase on these samples increased with the increasing DO of chitosan, with DD95 being the most easily hydrolyzed. Colloidal chitin was hardly hydrolyzed. The optimal reaction temperature and pH for cellulase digestion of chitosan were 55 deg C and pH 5.2. respectively. During cellulase digestion of chitosan, the 9-h hydrolysate had the highest enhancing effect on the proliferation of a human hybridoma cell, HB4C5. This hydrolysate is composed of low-molecular-weight chitosan (LMWC), with a molecular mass of 20.0 kDa, and chitoollgosaccharides, which are composed of sugars with a degree of polymerization of 1-6. In vitro, the 9-h hydrolysate increased both cell proliferation and immunoglobulin (lg)M secretion of HB4C5 because of the presence of chitooligosacchandes for the former activity and LMWC for the latter activity. In vivo, samples of the chitosan hydrolysate, chitooligosaccharide mixture and LMWC significantly increased the levels of serum lgG and 1gM, and enhanced concanavalin A- and lipopolysaccharide-induced proliferation of mouse lymphocytes. |
doi_str_mv | 10.1111/j.1444-2906.2004.00912.x |
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In vitro, the 9-h hydrolysate increased both cell proliferation and immunoglobulin (lg)M secretion of HB4C5 because of the presence of chitooligosacchandes for the former activity and LMWC for the latter activity. In vivo, samples of the chitosan hydrolysate, chitooligosaccharide mixture and LMWC significantly increased the levels of serum lgG and 1gM, and enhanced concanavalin A- and lipopolysaccharide-induced proliferation of mouse lymphocytes.</description><identifier>ISSN: 0919-9268</identifier><identifier>EISSN: 1444-2906</identifier><identifier>DOI: 10.1111/j.1444-2906.2004.00912.x</identifier><language>eng</language><publisher>Melbourne, Australia: Blackwell Science Pty</publisher><subject>CELL MEDIATED IMMUNITY ; CELLULASE ; Chitin ; chitooligosaccharides ; CHITOSAN ; chitosan hydrolysate ; DEGRADATION ; Feeds ; Fisheries ; hydrolytic activity ; immunoactivity ; IMMUNOGLOBULINS ; LIPOPOLYSACCHARIDES ; low‐molecular‐weight chitosan ; Lymphocytes ; PRAWNS AND SHRIMPS ; Shellfish</subject><ispartof>Fisheries science, 2004-12, Vol.70 (6), p.1113-1120</ispartof><rights>Copyright Blackwell Publishing Dec 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5682-b44930b8bd2be9e499677cecdb741d35ef42942ad85b732549ae8b7f6d7b0acf3</citedby><cites>FETCH-LOGICAL-c5682-b44930b8bd2be9e499677cecdb741d35ef42942ad85b732549ae8b7f6d7b0acf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1444-2906.2004.00912.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1444-2906.2004.00912.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Wu, G.J. (National Taiwan Ocean Univ., Keelung)</creatorcontrib><creatorcontrib>Tsai, G.J</creatorcontrib><title>Cellulase degradation of shrimp chitosan for the preparation of a water-soluble hydrolysate with immunoactivity</title><title>Fisheries science</title><description>Samples of colloidal chitin and chitosans with deacetylation degrees (DD) of 50, 65, 75 and 95% (DD5O, DD65, DD75 and DD95, respectively) were prepared from shrimp chitin. The hydrolytic activity of cellulase on these samples increased with the increasing DO of chitosan, with DD95 being the most easily hydrolyzed. Colloidal chitin was hardly hydrolyzed. The optimal reaction temperature and pH for cellulase digestion of chitosan were 55 deg C and pH 5.2. respectively. During cellulase digestion of chitosan, the 9-h hydrolysate had the highest enhancing effect on the proliferation of a human hybridoma cell, HB4C5. This hydrolysate is composed of low-molecular-weight chitosan (LMWC), with a molecular mass of 20.0 kDa, and chitoollgosaccharides, which are composed of sugars with a degree of polymerization of 1-6. In vitro, the 9-h hydrolysate increased both cell proliferation and immunoglobulin (lg)M secretion of HB4C5 because of the presence of chitooligosacchandes for the former activity and LMWC for the latter activity. In vivo, samples of the chitosan hydrolysate, chitooligosaccharide mixture and LMWC significantly increased the levels of serum lgG and 1gM, and enhanced concanavalin A- and lipopolysaccharide-induced proliferation of mouse lymphocytes.</description><subject>CELL MEDIATED IMMUNITY</subject><subject>CELLULASE</subject><subject>Chitin</subject><subject>chitooligosaccharides</subject><subject>CHITOSAN</subject><subject>chitosan hydrolysate</subject><subject>DEGRADATION</subject><subject>Feeds</subject><subject>Fisheries</subject><subject>hydrolytic activity</subject><subject>immunoactivity</subject><subject>IMMUNOGLOBULINS</subject><subject>LIPOPOLYSACCHARIDES</subject><subject>low‐molecular‐weight chitosan</subject><subject>Lymphocytes</subject><subject>PRAWNS AND SHRIMPS</subject><subject>Shellfish</subject><issn>0919-9268</issn><issn>1444-2906</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqNkUFr2zAUx8XoYGm3jzAQO_RmT5JlW4JeRmjajsIG7c5Csp9rBcfyJLuJv_3kpuSwU4RA4un3f_D0QwhTktK4vm9TyjlPmCRFygjhKSGSsvTwAa1ODxdoFYsykawQn9BlCFtCSJETsUJuDV03dToAruHF61qP1vXYNTi03u4GXLV2dEH3uHEejy3gwcOg_QnTeK9H8Elw3WQ6wO1ce9fNIRbx3o4ttrvd1DtdjfbVjvNn9LHRXYAv7-cV-rO5fV7fJ4-_7h7WPx6TKi8ESwznMiNGmJoZkMClLMqygqo2Jad1lkPDmeRM1yI3ZcZyLjUIUzZFXRqiqya7QtfHvoN3fycIo9rZUMVZdQ9uCoqWXIicknNAXgjBI_jtP3DrJt_HIRRjJZOZFEWExBGqvAvBQ6OG-Ivaz4oStfhSW7VoUYsWtfhSb77UIUZvjtG97WA-O6c2D0_xEuNfj_FGO6VfvA3q5-8I5svOaPYPVuGmQw</recordid><startdate>200412</startdate><enddate>200412</enddate><creator>Wu, G.J. (National Taiwan Ocean Univ., Keelung)</creator><creator>Tsai, G.J</creator><general>Blackwell Science Pty</general><general>Springer Nature B.V</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TN</scope><scope>7U7</scope><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>H98</scope><scope>L.G</scope><scope>8FD</scope><scope>FR3</scope><scope>H99</scope><scope>L.F</scope><scope>P64</scope></search><sort><creationdate>200412</creationdate><title>Cellulase degradation of shrimp chitosan for the preparation of a water-soluble hydrolysate with immunoactivity</title><author>Wu, G.J. (National Taiwan Ocean Univ., Keelung) ; Tsai, G.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5682-b44930b8bd2be9e499677cecdb741d35ef42942ad85b732549ae8b7f6d7b0acf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>CELL MEDIATED IMMUNITY</topic><topic>CELLULASE</topic><topic>Chitin</topic><topic>chitooligosaccharides</topic><topic>CHITOSAN</topic><topic>chitosan hydrolysate</topic><topic>DEGRADATION</topic><topic>Feeds</topic><topic>Fisheries</topic><topic>hydrolytic activity</topic><topic>immunoactivity</topic><topic>IMMUNOGLOBULINS</topic><topic>LIPOPOLYSACCHARIDES</topic><topic>low‐molecular‐weight chitosan</topic><topic>Lymphocytes</topic><topic>PRAWNS AND SHRIMPS</topic><topic>Shellfish</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, G.J. (National Taiwan Ocean Univ., Keelung)</creatorcontrib><creatorcontrib>Tsai, G.J</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>Oceanic Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Fisheries science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, G.J. (National Taiwan Ocean Univ., Keelung)</au><au>Tsai, G.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellulase degradation of shrimp chitosan for the preparation of a water-soluble hydrolysate with immunoactivity</atitle><jtitle>Fisheries science</jtitle><date>2004-12</date><risdate>2004</risdate><volume>70</volume><issue>6</issue><spage>1113</spage><epage>1120</epage><pages>1113-1120</pages><issn>0919-9268</issn><eissn>1444-2906</eissn><abstract>Samples of colloidal chitin and chitosans with deacetylation degrees (DD) of 50, 65, 75 and 95% (DD5O, DD65, DD75 and DD95, respectively) were prepared from shrimp chitin. The hydrolytic activity of cellulase on these samples increased with the increasing DO of chitosan, with DD95 being the most easily hydrolyzed. Colloidal chitin was hardly hydrolyzed. The optimal reaction temperature and pH for cellulase digestion of chitosan were 55 deg C and pH 5.2. respectively. During cellulase digestion of chitosan, the 9-h hydrolysate had the highest enhancing effect on the proliferation of a human hybridoma cell, HB4C5. This hydrolysate is composed of low-molecular-weight chitosan (LMWC), with a molecular mass of 20.0 kDa, and chitoollgosaccharides, which are composed of sugars with a degree of polymerization of 1-6. In vitro, the 9-h hydrolysate increased both cell proliferation and immunoglobulin (lg)M secretion of HB4C5 because of the presence of chitooligosacchandes for the former activity and LMWC for the latter activity. In vivo, samples of the chitosan hydrolysate, chitooligosaccharide mixture and LMWC significantly increased the levels of serum lgG and 1gM, and enhanced concanavalin A- and lipopolysaccharide-induced proliferation of mouse lymphocytes.</abstract><cop>Melbourne, Australia</cop><pub>Blackwell Science Pty</pub><doi>10.1111/j.1444-2906.2004.00912.x</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | CELL MEDIATED IMMUNITY CELLULASE Chitin chitooligosaccharides CHITOSAN chitosan hydrolysate DEGRADATION Feeds Fisheries hydrolytic activity immunoactivity IMMUNOGLOBULINS LIPOPOLYSACCHARIDES low‐molecular‐weight chitosan Lymphocytes PRAWNS AND SHRIMPS Shellfish |
title | Cellulase degradation of shrimp chitosan for the preparation of a water-soluble hydrolysate with immunoactivity |
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