UN METODO PARA EL DESARROLLO MOLECULAR IN VITRO DE UNA FUNCION PROTEICA
Un método para generar una secuencia de polinucleótidos o población de secuencias desde las secuencias de polinucleótido de filamento simple codificando una o más proteinas causales, el método comprende los pasos de: a) suministrar una primera población de moléculas de polinucleótidos de filamento s...
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description | Un método para generar una secuencia de polinucleótidos o población de secuencias desde las secuencias de polinucleótido de filamento simple codificando una o más proteinas causales, el método comprende los pasos de: a) suministrar una primera población de moléculas de polinucleótidos de filamento simple, la primera y segunda poblaciones juntas constituyen los filamentos positivos y negativos de la secuencia de polinucleótidos progenitores; b) realizar una reacción para la asimilación de las primera y segunda poblaciones de moléculas de polinucleótidos de filamento simple con una exonucleasa para generar las correspondientes poblaciones de fragmentos de polinucleótidos de filamento simple; c) contactar dichos fragmentos de polinucleótidos generados desde los filamentos positivos con fragmentos generados desde los filamentos negativos; y d) amplificar los fragmentos que templan a cada otro para generar al menos una secuencia de polinucleótidos codificando una o más proteínas causales que tienen características alteradas como se comparó con una o más proteinas causales codificadas por dichos polinucleótidos progenitores. en donde, en el paso (b), al menos un parámetro de la reacción usada para asimilación de la primera población de moléculas de polinucleótidos de filamento simple es diferente del parámetro(s) equivalente(s) usado(s) en la reacción para la asimilación de la segunda población de moléculas de polinucleótidos de filamento simple.
A method for in vitro molecular evolution of protein function The invention provides a method for generating a polynucleotide sequence or population of sequences from parent single-stranded polynucleotide sequences encoding one or more protein motifs, comprising the steps of (a) providing a first population of single-stranded polynucleotide molecules and a second population of single-stranded polynucleotide molecules, the first and second populations together constituting plus and minus strands of parent polynucleotide sequences, (b) carrying out a reaction for digesting the first and second populations of single-stranded polynucleotide molecules with an exonuclease to generate corresponding populations of single-stranded polynucleotide fragments, (c) contacting said fragments generated from the plus strands with fragments generated from the minus strands and optionally, adding primer sequences that anneal to the 3' and 5'ends of at least one of the parent polynucleotides under annealing conditions, and (d) amplifying t |
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fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_ES2285118TT5</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ES2285118TT5</sourcerecordid><originalsourceid>FETCH-epo_espacenet_ES2285118TT53</originalsourceid><addsrcrecordid>eNqNyjEKwkAQQNFtLES9w3gAi0QCaYfNRBc2O2EymzYEGSvRQLw_WngAq1-8v3WXnKAj5YahR0GgCA0NKMIxMnQcyeeIAiHBGFT4q5ATQpuTD5ygF1YKHvduc58fqx1-3bljS-qvJ1tek63LfLOnvScayrKuiqJWrc7_PB_ATyzG</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>UN METODO PARA EL DESARROLLO MOLECULAR IN VITRO DE UNA FUNCION PROTEICA</title><source>esp@cenet</source><creator>FUREBRING, CHRISTINA ; MALMBORG, HAGER ; CARLSSON, ROLAND ; BORREBAECK, CARL</creator><creatorcontrib>FUREBRING, CHRISTINA ; MALMBORG, HAGER ; CARLSSON, ROLAND ; BORREBAECK, CARL</creatorcontrib><description>Un método para generar una secuencia de polinucleótidos o población de secuencias desde las secuencias de polinucleótido de filamento simple codificando una o más proteinas causales, el método comprende los pasos de: a) suministrar una primera población de moléculas de polinucleótidos de filamento simple, la primera y segunda poblaciones juntas constituyen los filamentos positivos y negativos de la secuencia de polinucleótidos progenitores; b) realizar una reacción para la asimilación de las primera y segunda poblaciones de moléculas de polinucleótidos de filamento simple con una exonucleasa para generar las correspondientes poblaciones de fragmentos de polinucleótidos de filamento simple; c) contactar dichos fragmentos de polinucleótidos generados desde los filamentos positivos con fragmentos generados desde los filamentos negativos; y d) amplificar los fragmentos que templan a cada otro para generar al menos una secuencia de polinucleótidos codificando una o más proteínas causales que tienen características alteradas como se comparó con una o más proteinas causales codificadas por dichos polinucleótidos progenitores. en donde, en el paso (b), al menos un parámetro de la reacción usada para asimilación de la primera población de moléculas de polinucleótidos de filamento simple es diferente del parámetro(s) equivalente(s) usado(s) en la reacción para la asimilación de la segunda población de moléculas de polinucleótidos de filamento simple.
A method for in vitro molecular evolution of protein function The invention provides a method for generating a polynucleotide sequence or population of sequences from parent single-stranded polynucleotide sequences encoding one or more protein motifs, comprising the steps of (a) providing a first population of single-stranded polynucleotide molecules and a second population of single-stranded polynucleotide molecules, the first and second populations together constituting plus and minus strands of parent polynucleotide sequences, (b) carrying out a reaction for digesting the first and second populations of single-stranded polynucleotide molecules with an exonuclease to generate corresponding populations of single-stranded polynucleotide fragments, (c) contacting said fragments generated from the plus strands with fragments generated from the minus strands and optionally, adding primer sequences that anneal to the 3' and 5'ends of at least one of the parent polynucleotides under annealing conditions, and (d) amplifying the fragments that anneal to each other to generate at least one polynucleotide sequence encoding one or more protein motifs having altered characteristics as compared to the one or more protein motifs encoded by said parent polynucleotides, wherein, in step (b), at least one parameter of the reaction used for digestion of the first population of single-stranded polynucleotide molecules is different from the equivalent parameter(s) used in the reaction for digestion of the second population of single-stranded polynucleotide molecules. Preferably, the reaction parameter is selected from exonuclease type, exonuclease concentration, reaction volume, duration of the digestion reaction, temperature of the reaction mixture, pH of the reaction mixture, length of parent single-stranded polynucleotide sequences, amount of single-stranded polynucleotide molecules and buffer composition of the reaction mixture.</description><language>spa</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS OR TEST PAPERS THEREFOR ; COMPOSITIONS THEREOF ; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES ; CULTURE MEDIA ; ENZYMOLOGY ; FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE ; HUMAN NECESSITIES ; HYGIENE ; MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; ORGANIC CHEMISTRY ; PEPTIDES ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; PROCESSES OF PREPARING SUCH COMPOSITIONS ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>2012</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20120921&DB=EPODOC&CC=ES&NR=2285118T5$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,778,883,25551,76304</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20120921&DB=EPODOC&CC=ES&NR=2285118T5$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>FUREBRING, CHRISTINA</creatorcontrib><creatorcontrib>MALMBORG, HAGER</creatorcontrib><creatorcontrib>CARLSSON, ROLAND</creatorcontrib><creatorcontrib>BORREBAECK, CARL</creatorcontrib><title>UN METODO PARA EL DESARROLLO MOLECULAR IN VITRO DE UNA FUNCION PROTEICA</title><description>Un método para generar una secuencia de polinucleótidos o población de secuencias desde las secuencias de polinucleótido de filamento simple codificando una o más proteinas causales, el método comprende los pasos de: a) suministrar una primera población de moléculas de polinucleótidos de filamento simple, la primera y segunda poblaciones juntas constituyen los filamentos positivos y negativos de la secuencia de polinucleótidos progenitores; b) realizar una reacción para la asimilación de las primera y segunda poblaciones de moléculas de polinucleótidos de filamento simple con una exonucleasa para generar las correspondientes poblaciones de fragmentos de polinucleótidos de filamento simple; c) contactar dichos fragmentos de polinucleótidos generados desde los filamentos positivos con fragmentos generados desde los filamentos negativos; y d) amplificar los fragmentos que templan a cada otro para generar al menos una secuencia de polinucleótidos codificando una o más proteínas causales que tienen características alteradas como se comparó con una o más proteinas causales codificadas por dichos polinucleótidos progenitores. en donde, en el paso (b), al menos un parámetro de la reacción usada para asimilación de la primera población de moléculas de polinucleótidos de filamento simple es diferente del parámetro(s) equivalente(s) usado(s) en la reacción para la asimilación de la segunda población de moléculas de polinucleótidos de filamento simple.
A method for in vitro molecular evolution of protein function The invention provides a method for generating a polynucleotide sequence or population of sequences from parent single-stranded polynucleotide sequences encoding one or more protein motifs, comprising the steps of (a) providing a first population of single-stranded polynucleotide molecules and a second population of single-stranded polynucleotide molecules, the first and second populations together constituting plus and minus strands of parent polynucleotide sequences, (b) carrying out a reaction for digesting the first and second populations of single-stranded polynucleotide molecules with an exonuclease to generate corresponding populations of single-stranded polynucleotide fragments, (c) contacting said fragments generated from the plus strands with fragments generated from the minus strands and optionally, adding primer sequences that anneal to the 3' and 5'ends of at least one of the parent polynucleotides under annealing conditions, and (d) amplifying the fragments that anneal to each other to generate at least one polynucleotide sequence encoding one or more protein motifs having altered characteristics as compared to the one or more protein motifs encoded by said parent polynucleotides, wherein, in step (b), at least one parameter of the reaction used for digestion of the first population of single-stranded polynucleotide molecules is different from the equivalent parameter(s) used in the reaction for digestion of the second population of single-stranded polynucleotide molecules. Preferably, the reaction parameter is selected from exonuclease type, exonuclease concentration, reaction volume, duration of the digestion reaction, temperature of the reaction mixture, pH of the reaction mixture, length of parent single-stranded polynucleotide sequences, amount of single-stranded polynucleotide molecules and buffer composition of the reaction mixture.</description><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS OR TEST PAPERS THEREFOR</subject><subject>COMPOSITIONS THEREOF</subject><subject>CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES</subject><subject>CULTURE MEDIA</subject><subject>ENZYMOLOGY</subject><subject>FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MICROORGANISMS OR ENZYMES</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>ORGANIC CHEMISTRY</subject><subject>PEPTIDES</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><subject>PROCESSES OF PREPARING SUCH COMPOSITIONS</subject><subject>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2012</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNyjEKwkAQQNFtLES9w3gAi0QCaYfNRBc2O2EymzYEGSvRQLw_WngAq1-8v3WXnKAj5YahR0GgCA0NKMIxMnQcyeeIAiHBGFT4q5ATQpuTD5ygF1YKHvduc58fqx1-3bljS-qvJ1tek63LfLOnvScayrKuiqJWrc7_PB_ATyzG</recordid><startdate>20120921</startdate><enddate>20120921</enddate><creator>FUREBRING, CHRISTINA</creator><creator>MALMBORG, HAGER</creator><creator>CARLSSON, ROLAND</creator><creator>BORREBAECK, CARL</creator><scope>EVB</scope></search><sort><creationdate>20120921</creationdate><title>UN METODO PARA EL DESARROLLO MOLECULAR IN VITRO DE UNA FUNCION PROTEICA</title><author>FUREBRING, CHRISTINA ; MALMBORG, HAGER ; CARLSSON, ROLAND ; BORREBAECK, CARL</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ES2285118TT53</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>spa</language><creationdate>2012</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS OR TEST PAPERS THEREFOR</topic><topic>COMPOSITIONS THEREOF</topic><topic>CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>ORGANIC CHEMISTRY</topic><topic>PEPTIDES</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><topic>PROCESSES OF PREPARING SUCH COMPOSITIONS</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>FUREBRING, CHRISTINA</creatorcontrib><creatorcontrib>MALMBORG, HAGER</creatorcontrib><creatorcontrib>CARLSSON, ROLAND</creatorcontrib><creatorcontrib>BORREBAECK, CARL</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>FUREBRING, CHRISTINA</au><au>MALMBORG, HAGER</au><au>CARLSSON, ROLAND</au><au>BORREBAECK, CARL</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>UN METODO PARA EL DESARROLLO MOLECULAR IN VITRO DE UNA FUNCION PROTEICA</title><date>2012-09-21</date><risdate>2012</risdate><abstract>Un método para generar una secuencia de polinucleótidos o población de secuencias desde las secuencias de polinucleótido de filamento simple codificando una o más proteinas causales, el método comprende los pasos de: a) suministrar una primera población de moléculas de polinucleótidos de filamento simple, la primera y segunda poblaciones juntas constituyen los filamentos positivos y negativos de la secuencia de polinucleótidos progenitores; b) realizar una reacción para la asimilación de las primera y segunda poblaciones de moléculas de polinucleótidos de filamento simple con una exonucleasa para generar las correspondientes poblaciones de fragmentos de polinucleótidos de filamento simple; c) contactar dichos fragmentos de polinucleótidos generados desde los filamentos positivos con fragmentos generados desde los filamentos negativos; y d) amplificar los fragmentos que templan a cada otro para generar al menos una secuencia de polinucleótidos codificando una o más proteínas causales que tienen características alteradas como se comparó con una o más proteinas causales codificadas por dichos polinucleótidos progenitores. en donde, en el paso (b), al menos un parámetro de la reacción usada para asimilación de la primera población de moléculas de polinucleótidos de filamento simple es diferente del parámetro(s) equivalente(s) usado(s) en la reacción para la asimilación de la segunda población de moléculas de polinucleótidos de filamento simple.
A method for in vitro molecular evolution of protein function The invention provides a method for generating a polynucleotide sequence or population of sequences from parent single-stranded polynucleotide sequences encoding one or more protein motifs, comprising the steps of (a) providing a first population of single-stranded polynucleotide molecules and a second population of single-stranded polynucleotide molecules, the first and second populations together constituting plus and minus strands of parent polynucleotide sequences, (b) carrying out a reaction for digesting the first and second populations of single-stranded polynucleotide molecules with an exonuclease to generate corresponding populations of single-stranded polynucleotide fragments, (c) contacting said fragments generated from the plus strands with fragments generated from the minus strands and optionally, adding primer sequences that anneal to the 3' and 5'ends of at least one of the parent polynucleotides under annealing conditions, and (d) amplifying the fragments that anneal to each other to generate at least one polynucleotide sequence encoding one or more protein motifs having altered characteristics as compared to the one or more protein motifs encoded by said parent polynucleotides, wherein, in step (b), at least one parameter of the reaction used for digestion of the first population of single-stranded polynucleotide molecules is different from the equivalent parameter(s) used in the reaction for digestion of the second population of single-stranded polynucleotide molecules. Preferably, the reaction parameter is selected from exonuclease type, exonuclease concentration, reaction volume, duration of the digestion reaction, temperature of the reaction mixture, pH of the reaction mixture, length of parent single-stranded polynucleotide sequences, amount of single-stranded polynucleotide molecules and buffer composition of the reaction mixture.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS OR TEST PAPERS THEREFOR COMPOSITIONS THEREOF CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES CULTURE MEDIA ENZYMOLOGY FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIREDCHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERSFROM A RACEMIC MIXTURE HUMAN NECESSITIES HYGIENE MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS MEDICAL OR VETERINARY SCIENCE METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING ORGANIC CHEMISTRY PEPTIDES PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES PROCESSES OF PREPARING SUCH COMPOSITIONS PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPIRITS VINEGAR WINE |
title | UN METODO PARA EL DESARROLLO MOLECULAR IN VITRO DE UNA FUNCION PROTEICA |
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