Characterization of enzymatically prepared biosurfactants

Various fatty monoesters of sugars and sugar alcohols were prepared enzymatically in organic solvent. Water produced during esterification was removed by refluxing through a dessicant under reduced pressure. Surface properties of these esters such as surface and interfacial tensions and their abilit...

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Veröffentlicht in:Journal of the American Oil Chemists' Society 1996-01, Vol.73 (1), p.109-113
Hauptverfasser: Ducret, A. (Biotechnology Research Institute, Montreal, Quebec, Canada.), Giroux, A
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container_title Journal of the American Oil Chemists' Society
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creator Ducret, A. (Biotechnology Research Institute, Montreal, Quebec, Canada.)
Giroux, A
description Various fatty monoesters of sugars and sugar alcohols were prepared enzymatically in organic solvent. Water produced during esterification was removed by refluxing through a dessicant under reduced pressure. Surface properties of these esters such as surface and interfacial tensions and their ability to stabilize emulsions at 30°C were evaluated: oleate esters of glucose, fructose, and sorbitol show similar behavior in reduction of surface and interfacial tensions, and values for the critical micelle concentration are about 8·10−5 M. It was also observed with sorbitol esters that the shorter the alkyl chain, the higher the critical micelle concentration. Generally, emulsions prepared with the emulsifier dissolved in the water or in the oil phase lead to oil‐in‐water or water‐in‐oil emulsions, respectively. Sorbitol monolaurate significantly increased the stability of oil‐in‐water emulsions, with only 5% separation of the phases after 48h at 30°C, compared to 10% for chemically prepared sorbitan monolaurate under the same conditions. Sorbitol monoerucate was very efficient in stabilizing water‐in‐oil emulsions, with only 1% separation of the phases.
doi_str_mv 10.1007/BF02523456
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Generally, emulsions prepared with the emulsifier dissolved in the water or in the oil phase lead to oil‐in‐water or water‐in‐oil emulsions, respectively. Sorbitol monolaurate significantly increased the stability of oil‐in‐water emulsions, with only 5% separation of the phases after 48h at 30°C, compared to 10% for chemically prepared sorbitan monolaurate under the same conditions. Sorbitol monoerucate was very efficient in stabilizing water‐in‐oil emulsions, with only 1% separation of the phases.</description><identifier>ISSN: 0003-021X</identifier><identifier>EISSN: 1558-9331</identifier><identifier>DOI: 10.1007/BF02523456</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>ACIDE GRAS ; ACIDOS GRASOS ; AZUCARES ; AZUCARES ALCOHOLES ; Bioconversions. 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Generally, emulsions prepared with the emulsifier dissolved in the water or in the oil phase lead to oil‐in‐water or water‐in‐oil emulsions, respectively. Sorbitol monolaurate significantly increased the stability of oil‐in‐water emulsions, with only 5% separation of the phases after 48h at 30°C, compared to 10% for chemically prepared sorbitan monolaurate under the same conditions. Sorbitol monoerucate was very efficient in stabilizing water‐in‐oil emulsions, with only 1% separation of the phases.</description><subject>ACIDE GRAS</subject><subject>ACIDOS GRASOS</subject><subject>AZUCARES</subject><subject>AZUCARES ALCOHOLES</subject><subject>Bioconversions. Hemisynthesis</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Critical micelle concentration</subject><subject>emulsifier emulsion stability</subject><subject>EMULSION</subject><subject>EMULSIONS</subject><subject>enzymatic esterification</subject><subject>ESTER</subject><subject>ESTERES</subject><subject>ESTERIFICACION</subject><subject>ESTERIFICATION</subject><subject>ESTERS</subject><subject>FATTY ACIDS</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>interfacial tension</subject><subject>lipase</subject><subject>Methods. Procedures. 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Hemisynthesis</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Critical micelle concentration</topic><topic>emulsifier emulsion stability</topic><topic>EMULSION</topic><topic>EMULSIONS</topic><topic>enzymatic esterification</topic><topic>ESTER</topic><topic>ESTERES</topic><topic>ESTERIFICACION</topic><topic>ESTERIFICATION</topic><topic>ESTERS</topic><topic>FATTY ACIDS</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>interfacial tension</topic><topic>lipase</topic><topic>Methods. Procedures. Technologies</topic><topic>nonionic surfactant</topic><topic>NONIONIC SURFACTANTS</topic><topic>STABILITY</topic><topic>SUCRE ALCOOL</topic><topic>SUCRES</topic><topic>sugar alcohol esters</topic><topic>SUGAR ALCOHOLS</topic><topic>sugar esters</topic><topic>SUGARS</topic><topic>SURFACE ACTIVE AGENTS</topic><topic>surface activity</topic><topic>SURFACE TENSION</topic><topic>SURFACTANT</topic><topic>SURFACTANTES</topic><topic>TENSION DE LA SUPERFICIE</topic><topic>TENSION SUPERFICIELLE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ducret, A. (Biotechnology Research Institute, Montreal, Quebec, Canada.)</creatorcontrib><creatorcontrib>Giroux, A</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of the American Oil Chemists' Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ducret, A. (Biotechnology Research Institute, Montreal, Quebec, Canada.)</au><au>Giroux, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of enzymatically prepared biosurfactants</atitle><jtitle>Journal of the American Oil Chemists' Society</jtitle><date>1996-01</date><risdate>1996</risdate><volume>73</volume><issue>1</issue><spage>109</spage><epage>113</epage><pages>109-113</pages><issn>0003-021X</issn><eissn>1558-9331</eissn><abstract>Various fatty monoesters of sugars and sugar alcohols were prepared enzymatically in organic solvent. Water produced during esterification was removed by refluxing through a dessicant under reduced pressure. Surface properties of these esters such as surface and interfacial tensions and their ability to stabilize emulsions at 30°C were evaluated: oleate esters of glucose, fructose, and sorbitol show similar behavior in reduction of surface and interfacial tensions, and values for the critical micelle concentration are about 8·10−5 M. It was also observed with sorbitol esters that the shorter the alkyl chain, the higher the critical micelle concentration. Generally, emulsions prepared with the emulsifier dissolved in the water or in the oil phase lead to oil‐in‐water or water‐in‐oil emulsions, respectively. Sorbitol monolaurate significantly increased the stability of oil‐in‐water emulsions, with only 5% separation of the phases after 48h at 30°C, compared to 10% for chemically prepared sorbitan monolaurate under the same conditions. Sorbitol monoerucate was very efficient in stabilizing water‐in‐oil emulsions, with only 1% separation of the phases.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><doi>10.1007/BF02523456</doi><tpages>5</tpages></addata></record>
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source Springer Nature - Complete Springer Journals; Wiley Online Library Journals Frontfile Complete
subjects ACIDE GRAS
ACIDOS GRASOS
AZUCARES
AZUCARES ALCOHOLES
Bioconversions. Hemisynthesis
Biological and medical sciences
Biotechnology
Critical micelle concentration
emulsifier emulsion stability
EMULSION
EMULSIONS
enzymatic esterification
ESTER
ESTERES
ESTERIFICACION
ESTERIFICATION
ESTERS
FATTY ACIDS
Fundamental and applied biological sciences. Psychology
interfacial tension
lipase
Methods. Procedures. Technologies
nonionic surfactant
NONIONIC SURFACTANTS
STABILITY
SUCRE ALCOOL
SUCRES
sugar alcohol esters
SUGAR ALCOHOLS
sugar esters
SUGARS
SURFACE ACTIVE AGENTS
surface activity
SURFACE TENSION
SURFACTANT
SURFACTANTES
TENSION DE LA SUPERFICIE
TENSION SUPERFICIELLE
title Characterization of enzymatically prepared biosurfactants
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