Preparation of immobilized invertase
Immobilized invertase was prepared by ionically binding the enzyme to diethylaminoacetyl cellulose (DEAA‐cellulose). DEAA‐cellulose‐invertase complex was quite stable to electrolyte in the range of pH 5–7. Bound invertase was less active than the native enzyme, and approximately 55–70% of the enzyme...
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Veröffentlicht in: | Biotechnology and bioengineering 1973-03, Vol.15 (2), p.403-412 |
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creator | Maeda, Hidekatsu Suzuki, Hideo Sakimae, Akihiro |
description | Immobilized invertase was prepared by ionically binding the enzyme to diethylaminoacetyl cellulose (DEAA‐cellulose). DEAA‐cellulose‐invertase complex was quite stable to electrolyte in the range of pH 5–7. Bound invertase was less active than the native enzyme, and approximately 55–70% of the enzyme activity was lost on binding. The complex was stable for 9 days' continuous inversion in a column system at 30°C, but was rather unstable at 40°C. Heat stability and the effect of temperature on the reaction rate of the complex were almost identical with those of the native enzyme. |
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DEAA‐cellulose‐invertase complex was quite stable to electrolyte in the range of pH 5–7. Bound invertase was less active than the native enzyme, and approximately 55–70% of the enzyme activity was lost on binding. The complex was stable for 9 days' continuous inversion in a column system at 30°C, but was rather unstable at 40°C. Heat stability and the effect of temperature on the reaction rate of the complex were almost identical with those of the native enzyme.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.260150214</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><ispartof>Biotechnology and bioengineering, 1973-03, Vol.15 (2), p.403-412</ispartof><rights>Copyright © 1973 John Wiley & Sons, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3234-25cb1383444c4cd4c9f3df0a1f48782537b6e38eefdf2e57c358095bd3b909d23</citedby><cites>FETCH-LOGICAL-c3234-25cb1383444c4cd4c9f3df0a1f48782537b6e38eefdf2e57c358095bd3b909d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbit.260150214$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbit.260150214$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Maeda, Hidekatsu</creatorcontrib><creatorcontrib>Suzuki, Hideo</creatorcontrib><creatorcontrib>Sakimae, Akihiro</creatorcontrib><title>Preparation of immobilized invertase</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol. Bioeng</addtitle><description>Immobilized invertase was prepared by ionically binding the enzyme to diethylaminoacetyl cellulose (DEAA‐cellulose). DEAA‐cellulose‐invertase complex was quite stable to electrolyte in the range of pH 5–7. Bound invertase was less active than the native enzyme, and approximately 55–70% of the enzyme activity was lost on binding. The complex was stable for 9 days' continuous inversion in a column system at 30°C, but was rather unstable at 40°C. Heat stability and the effect of temperature on the reaction rate of the complex were almost identical with those of the native enzyme.</description><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1973</creationdate><recordtype>article</recordtype><recordid>eNp9j0FLAzEQhYMouFaP3nvwunWSSTaboxZbi0WlrvQYstkEom23JItaf72VluLJ0_Dge2_4CLmkMKAA7LoO3YAVQAUwyo9IRkHJHJiCY5IBQJGjUOyUnKX0to2yLIqMXD1HtzbRdKFd9VvfD8tlW4dF-HZNP6w-XOxMcufkxJtFchf72yOvo7tqeJ9Pn8aT4c00t8iQ50zYmmKJnHPLbcOt8th4MNTzUpZMoKwLh6VzvvHMCWlRlKBE3WCtQDUMeyTf7drYphSd1-sYliZuNAX9q6i3ivqguOXljv8MC7f5H9a3k-pvc_8ppM59HZomvutCohR6_jjWMB1V85fZg57hD8B_Ywg</recordid><startdate>197303</startdate><enddate>197303</enddate><creator>Maeda, Hidekatsu</creator><creator>Suzuki, Hideo</creator><creator>Sakimae, Akihiro</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>197303</creationdate><title>Preparation of immobilized invertase</title><author>Maeda, Hidekatsu ; Suzuki, Hideo ; Sakimae, Akihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3234-25cb1383444c4cd4c9f3df0a1f48782537b6e38eefdf2e57c358095bd3b909d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1973</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maeda, Hidekatsu</creatorcontrib><creatorcontrib>Suzuki, Hideo</creatorcontrib><creatorcontrib>Sakimae, Akihiro</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Biotechnology and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maeda, Hidekatsu</au><au>Suzuki, Hideo</au><au>Sakimae, Akihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation of immobilized invertase</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>1973-03</date><risdate>1973</risdate><volume>15</volume><issue>2</issue><spage>403</spage><epage>412</epage><pages>403-412</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><abstract>Immobilized invertase was prepared by ionically binding the enzyme to diethylaminoacetyl cellulose (DEAA‐cellulose). DEAA‐cellulose‐invertase complex was quite stable to electrolyte in the range of pH 5–7. Bound invertase was less active than the native enzyme, and approximately 55–70% of the enzyme activity was lost on binding. The complex was stable for 9 days' continuous inversion in a column system at 30°C, but was rather unstable at 40°C. Heat stability and the effect of temperature on the reaction rate of the complex were almost identical with those of the native enzyme.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/bit.260150214</doi><tpages>10</tpages></addata></record> |
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title | Preparation of immobilized invertase |
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