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Effect of temperature on the synthesis, composition and physical properties of potato starch
Potato tubers (cv Maris Piper) were grown at 10, 16, 20 and 25 degrees C in constant-environment chambers until maturity, whereupon the starches were extracted and subjected to rigorous chemical and physical analysis. The structure of the amylopectin molecules from the different starches postdebranc...
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Published in: | Journal of the science of food and agriculture 1999-11, Vol.79 (14), p.2045-2051 |
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description | Potato tubers (cv Maris Piper) were grown at 10, 16, 20 and 25 degrees C in constant-environment chambers until maturity, whereupon the starches were extracted and subjected to rigorous chemical and physical analysis. The structure of the amylopectin molecules from the different starches postdebranching with isoamylase showed very little variation. The amylose and phosphorus content of the starches did show some variability while granule size tended to decrease as growth temperature was increased. There was, however, a marked increase in gelatinisation temperatures with a roughly constant enthalpy of gelatinisation as a function of growth temperature. The number of amylopectin double helices was determined by (13)C CPLMAS-NMR and crystallinity by wide-angle X-ray diffraction and in common with the enthalpy of gelatinisation found to be almost constant. It is proposed that the differences in the gelatinisation temperatures reflect enhanced registration of the amylopectin double helices in crystallites which restricts hydration and hence elevates gelatinisation temperatures. This is probably associated with enhanced rigidity of amorphous regions. The consequence of these ordering effects is that sweding is restricted, even if there is no detectable order by DSC (post-T(c)), because of steric hindrance to hydration exerted by the closer proximity/improved registration of the amylopectin chains. |
doi_str_mv | 10.1002/(SICI)1097-0010(199911)79:14<2045::AID-JSFA488>3.0.CO;2-V |
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The structure of the amylopectin molecules from the different starches postdebranching with isoamylase showed very little variation. The amylose and phosphorus content of the starches did show some variability while granule size tended to decrease as growth temperature was increased. There was, however, a marked increase in gelatinisation temperatures with a roughly constant enthalpy of gelatinisation as a function of growth temperature. The number of amylopectin double helices was determined by (13)C CPLMAS-NMR and crystallinity by wide-angle X-ray diffraction and in common with the enthalpy of gelatinisation found to be almost constant. It is proposed that the differences in the gelatinisation temperatures reflect enhanced registration of the amylopectin double helices in crystallites which restricts hydration and hence elevates gelatinisation temperatures. This is probably associated with enhanced rigidity of amorphous regions. The consequence of these ordering effects is that sweding is restricted, even if there is no detectable order by DSC (post-T(c)), because of steric hindrance to hydration exerted by the closer proximity/improved registration of the amylopectin chains.</description><identifier>ISSN: 0022-5142</identifier><identifier>EISSN: 1097-0010</identifier><identifier>DOI: 10.1002/(SICI)1097-0010(199911)79:14<2045::AID-JSFA488>3.0.CO;2-V</identifier><identifier>CODEN: JSFAAE</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>air temperature ; ambient temperature ; amylopectin ; amylose ; amylose double helices ; annealing ; Biological and medical sciences ; chemical composition ; chemical structure ; crystallization ; debranching ; enthalpy ; Food industries ; Fundamental and applied biological sciences. Psychology ; gelatinisation ; gelation ; growth ; growth temperature ; molecular conformation ; nuclear magnetic resonance spectroscopy ; phosphorus ; potato starch ; potato tubers ; Solanum tuberosum ; starch ; Starch and starchy product industries ; temperature ; thermodynamics ; X-ray diffraction</subject><ispartof>Journal of the science of food and agriculture, 1999-11, Vol.79 (14), p.2045-2051</ispartof><rights>Copyright © 1999 Society of Chemical Industry</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4398-8e5ebbf02faddb2c4129d92eb98ce88028c2e50243049eeb0f11c214f0de44263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1225169$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Tester, R.F</creatorcontrib><creatorcontrib>Debon, S.J.J</creatorcontrib><creatorcontrib>Davies, H.V</creatorcontrib><creatorcontrib>Gidley, M.J</creatorcontrib><title>Effect of temperature on the synthesis, composition and physical properties of potato starch</title><title>Journal of the science of food and agriculture</title><addtitle>J. Sci. Food Agric</addtitle><description>Potato tubers (cv Maris Piper) were grown at 10, 16, 20 and 25 degrees C in constant-environment chambers until maturity, whereupon the starches were extracted and subjected to rigorous chemical and physical analysis. The structure of the amylopectin molecules from the different starches postdebranching with isoamylase showed very little variation. The amylose and phosphorus content of the starches did show some variability while granule size tended to decrease as growth temperature was increased. There was, however, a marked increase in gelatinisation temperatures with a roughly constant enthalpy of gelatinisation as a function of growth temperature. The number of amylopectin double helices was determined by (13)C CPLMAS-NMR and crystallinity by wide-angle X-ray diffraction and in common with the enthalpy of gelatinisation found to be almost constant. It is proposed that the differences in the gelatinisation temperatures reflect enhanced registration of the amylopectin double helices in crystallites which restricts hydration and hence elevates gelatinisation temperatures. This is probably associated with enhanced rigidity of amorphous regions. The consequence of these ordering effects is that sweding is restricted, even if there is no detectable order by DSC (post-T(c)), because of steric hindrance to hydration exerted by the closer proximity/improved registration of the amylopectin chains.</description><subject>air temperature</subject><subject>ambient temperature</subject><subject>amylopectin</subject><subject>amylose</subject><subject>amylose double helices</subject><subject>annealing</subject><subject>Biological and medical sciences</subject><subject>chemical composition</subject><subject>chemical structure</subject><subject>crystallization</subject><subject>debranching</subject><subject>enthalpy</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gelatinisation</subject><subject>gelation</subject><subject>growth</subject><subject>growth temperature</subject><subject>molecular conformation</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>phosphorus</subject><subject>potato starch</subject><subject>potato tubers</subject><subject>Solanum tuberosum</subject><subject>starch</subject><subject>Starch and starchy product industries</subject><subject>temperature</subject><subject>thermodynamics</subject><subject>X-ray diffraction</subject><issn>0022-5142</issn><issn>1097-0010</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkF1v0zAUhiMEEmXwG4gEF5tEyrHjJHZBSFX2QWHQi7IhpklHjmPTjLbJbFej_x5HKeMCJK4s2e953uMniqYExgSAvj5czMrZEQFRJAAEDokQgpCjQkwIe0uBZZPJdHacfFicThnn79IxjMv5G5pcPohG91MPo1Fg0SQjjD6Onjh3AwBC5Pkouj4xRisftyb2et1pK_3W6rjdxH6pY7fbhMM17lWs2nXXusY34Ulu6rhb7lyj5CrubBvGfKNdD-laL30bOy-tWj6NHhm5cvrZ_jyILk5PvpTvk_P52aycnieKpYInXGe6qgxQI-u6oooRKmpBdSW40pwD5YrqDChLgQmtKzCEKEqYgVozRvP0IHoxcMMut1vtPN60W7sJlUh4Gj7KGach9W1IKds6Z7XBzjZraXdIAHvZiL1s7LVhrw0H2VgIJAx72YhBNu5lY4qA5RwpXgb2y_0G0gUpxsqNatyfAkozkosQux5id81K7_7q_2_9v9t_XwV8MuAb5_XPe7y0PzAv0iLDr5_PkF9lxx_TK4afQv75kDeyRfndho0vFhRIClRknGQs_QUO0Lla</recordid><startdate>199911</startdate><enddate>199911</enddate><creator>Tester, R.F</creator><creator>Debon, S.J.J</creator><creator>Davies, H.V</creator><creator>Gidley, M.J</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><general>Published for the Society of Chemical Industry by Elsevier Applied Science</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>HJHVS</scope><scope>IZSXY</scope><scope>K30</scope><scope>PAAUG</scope><scope>PAWHS</scope><scope>PAWZZ</scope><scope>PAXOH</scope><scope>PBHAV</scope><scope>PBQSW</scope><scope>PBYQZ</scope><scope>PCIWU</scope><scope>PCMID</scope><scope>PCZJX</scope><scope>PDGRG</scope><scope>PDWWI</scope><scope>PETMR</scope><scope>PFVGT</scope><scope>PGXDX</scope><scope>PIHIL</scope><scope>PISVA</scope><scope>PJCTQ</scope><scope>PJTMS</scope><scope>PLCHJ</scope><scope>PMHAD</scope><scope>PNQDJ</scope><scope>POUND</scope><scope>PPLAD</scope><scope>PQAPC</scope><scope>PQCAN</scope><scope>PQCMW</scope><scope>PQEME</scope><scope>PQHKH</scope><scope>PQMID</scope><scope>PQNCT</scope><scope>PQNET</scope><scope>PQSCT</scope><scope>PQSET</scope><scope>PSVJG</scope><scope>PVMQY</scope><scope>PZGFC</scope></search><sort><creationdate>199911</creationdate><title>Effect of temperature on the synthesis, composition and physical properties of potato starch</title><author>Tester, R.F ; Debon, S.J.J ; Davies, H.V ; Gidley, M.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4398-8e5ebbf02faddb2c4129d92eb98ce88028c2e50243049eeb0f11c214f0de44263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>air temperature</topic><topic>ambient temperature</topic><topic>amylopectin</topic><topic>amylose</topic><topic>amylose double helices</topic><topic>annealing</topic><topic>Biological and medical sciences</topic><topic>chemical composition</topic><topic>chemical structure</topic><topic>crystallization</topic><topic>debranching</topic><topic>enthalpy</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gelatinisation</topic><topic>gelation</topic><topic>growth</topic><topic>growth temperature</topic><topic>molecular conformation</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>phosphorus</topic><topic>potato starch</topic><topic>potato tubers</topic><topic>Solanum tuberosum</topic><topic>starch</topic><topic>Starch and starchy product industries</topic><topic>temperature</topic><topic>thermodynamics</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tester, R.F</creatorcontrib><creatorcontrib>Debon, S.J.J</creatorcontrib><creatorcontrib>Davies, H.V</creatorcontrib><creatorcontrib>Gidley, M.J</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Periodicals Index Online Segment 19</collection><collection>Periodicals Index Online Segment 30</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Midwest</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Northeast</collection><collection>Primary Sources Access (Plan D) - Southeast</collection><collection>Primary Sources Access (Plan D) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Southeast</collection><collection>Primary Sources Access (Plan D) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - UK / I</collection><collection>Primary Sources Access (Plan D) - Canada</collection><collection>Primary Sources Access (Plan D) - EMEALA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - International</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - International</collection><collection>Primary Sources Access (Plan D) - West</collection><collection>Periodicals Index Online Segments 1-50</collection><collection>Primary Sources Access (Plan D) - APAC</collection><collection>Primary Sources Access (Plan D) - Midwest</collection><collection>Primary Sources Access (Plan D) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Canada</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - EMEALA</collection><collection>Primary Sources Access & Build (Plan A) - APAC</collection><collection>Primary Sources Access & Build (Plan A) - Canada</collection><collection>Primary Sources Access & Build (Plan A) - West</collection><collection>Primary Sources Access & Build (Plan A) - EMEALA</collection><collection>Primary Sources Access (Plan D) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - Midwest</collection><collection>Primary Sources Access & Build (Plan A) - North Central</collection><collection>Primary Sources Access & Build (Plan A) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - Southeast</collection><collection>Primary Sources Access (Plan D) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - APAC</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - MEA</collection><jtitle>Journal of the science of food and agriculture</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tester, R.F</au><au>Debon, S.J.J</au><au>Davies, H.V</au><au>Gidley, M.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of temperature on the synthesis, composition and physical properties of potato starch</atitle><jtitle>Journal of the science of food and agriculture</jtitle><addtitle>J. Sci. Food Agric</addtitle><date>1999-11</date><risdate>1999</risdate><volume>79</volume><issue>14</issue><spage>2045</spage><epage>2051</epage><pages>2045-2051</pages><issn>0022-5142</issn><eissn>1097-0010</eissn><coden>JSFAAE</coden><abstract>Potato tubers (cv Maris Piper) were grown at 10, 16, 20 and 25 degrees C in constant-environment chambers until maturity, whereupon the starches were extracted and subjected to rigorous chemical and physical analysis. The structure of the amylopectin molecules from the different starches postdebranching with isoamylase showed very little variation. The amylose and phosphorus content of the starches did show some variability while granule size tended to decrease as growth temperature was increased. There was, however, a marked increase in gelatinisation temperatures with a roughly constant enthalpy of gelatinisation as a function of growth temperature. The number of amylopectin double helices was determined by (13)C CPLMAS-NMR and crystallinity by wide-angle X-ray diffraction and in common with the enthalpy of gelatinisation found to be almost constant. It is proposed that the differences in the gelatinisation temperatures reflect enhanced registration of the amylopectin double helices in crystallites which restricts hydration and hence elevates gelatinisation temperatures. This is probably associated with enhanced rigidity of amorphous regions. The consequence of these ordering effects is that sweding is restricted, even if there is no detectable order by DSC (post-T(c)), because of steric hindrance to hydration exerted by the closer proximity/improved registration of the amylopectin chains.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/(SICI)1097-0010(199911)79:14<2045::AID-JSFA488>3.0.CO;2-V</doi><tpages>7</tpages></addata></record> |
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subjects | air temperature ambient temperature amylopectin amylose amylose double helices annealing Biological and medical sciences chemical composition chemical structure crystallization debranching enthalpy Food industries Fundamental and applied biological sciences. Psychology gelatinisation gelation growth growth temperature molecular conformation nuclear magnetic resonance spectroscopy phosphorus potato starch potato tubers Solanum tuberosum starch Starch and starchy product industries temperature thermodynamics X-ray diffraction |
title | Effect of temperature on the synthesis, composition and physical properties of potato starch |
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