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Application of solution equilibrium analysis to in vitro RNA transcription
Solution equilibrium analysis of in vitro RNA transcription has been applied to examine changes in pH, free magnesium concentration, and concentrations of all chemical ionization species as a transcription reaction proceeds. With this method, the progress of a transcription reaction can be accuratel...
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Published in: | Biotechnology progress 1997-11, Vol.13 (6), p.747-756 |
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container_title | Biotechnology progress |
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creator | KERN, J. A DAVIS, R. H |
description | Solution equilibrium analysis of in vitro RNA transcription has been applied to examine changes in pH, free magnesium concentration, and concentrations of all chemical ionization species as a transcription reaction proceeds. With this method, the progress of a transcription reaction can be accurately determined as a function of measured pH. In addition, it is demonstrated that this method has significant value as a tool for achieving improved understanding of the effects of varying solution conditions on the dynamics of RNA transcription. Magnesium concentration was found to be a critical factor for efficient transcription. Below 5 mM free Mg2+ concentration, the transcription rate and the efficiency at which nucleoside triphosphates (NTPs) are incorporated are greatly reduced. While inorganic pyrophosphate (PPi), a byproduct of the reaction, was found to directly inhibit the rate of transcription, its detrimental effects on transcription were determined to be primarily due to sequestering of magnesium. The PPi forms a precipitate with magnesium which was determined to have a molar composition of 2:1 of Mg:PPi. Transcription rate and efficiency of NTP incorporation are also reduced with increasing ionic strength. It is shown that these reductions can be partially alleviated by replacing chloride with acetate anions. |
doi_str_mv | 10.1021/bp970094p |
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A ; DAVIS, R. H</creator><creatorcontrib>KERN, J. A ; DAVIS, R. H</creatorcontrib><description>Solution equilibrium analysis of in vitro RNA transcription has been applied to examine changes in pH, free magnesium concentration, and concentrations of all chemical ionization species as a transcription reaction proceeds. With this method, the progress of a transcription reaction can be accurately determined as a function of measured pH. In addition, it is demonstrated that this method has significant value as a tool for achieving improved understanding of the effects of varying solution conditions on the dynamics of RNA transcription. Magnesium concentration was found to be a critical factor for efficient transcription. Below 5 mM free Mg2+ concentration, the transcription rate and the efficiency at which nucleoside triphosphates (NTPs) are incorporated are greatly reduced. While inorganic pyrophosphate (PPi), a byproduct of the reaction, was found to directly inhibit the rate of transcription, its detrimental effects on transcription were determined to be primarily due to sequestering of magnesium. The PPi forms a precipitate with magnesium which was determined to have a molar composition of 2:1 of Mg:PPi. Transcription rate and efficiency of NTP incorporation are also reduced with increasing ionic strength. It is shown that these reductions can be partially alleviated by replacing chloride with acetate anions.</description><identifier>ISSN: 8756-7938</identifier><identifier>EISSN: 1520-6033</identifier><identifier>DOI: 10.1021/bp970094p</identifier><identifier>PMID: 9413132</identifier><identifier>CODEN: BIPRET</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Base Sequence ; Biological and medical sciences ; Biotechnology ; Chemical Precipitation ; Diverse techniques ; DNA ; Fundamental and applied biological sciences. Psychology ; Genetic engineering ; Genetic technics ; Hydrogen-Ion Concentration ; Kinetics ; Magnesium - administration & dosage ; Magnesium - pharmacology ; Methods. Procedures. Technologies ; Miscellaneous ; Molecular and cellular biology ; Nucleotides - metabolism ; Osmolar Concentration ; Phosphates - metabolism ; RNA - genetics ; RNA - metabolism ; Solutions ; Synthetic digonucleotides and genes. Sequencing ; Templates, Genetic ; Transcription, Genetic</subject><ispartof>Biotechnology progress, 1997-11, Vol.13 (6), p.747-756</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-9469c6ddca971b40791eb577ebebc371ead2019a5fa29a9e70060b1f92c803463</citedby></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=2125380$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9413132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KERN, J. A</creatorcontrib><creatorcontrib>DAVIS, R. H</creatorcontrib><title>Application of solution equilibrium analysis to in vitro RNA transcription</title><title>Biotechnology progress</title><addtitle>Biotechnol Prog</addtitle><description>Solution equilibrium analysis of in vitro RNA transcription has been applied to examine changes in pH, free magnesium concentration, and concentrations of all chemical ionization species as a transcription reaction proceeds. With this method, the progress of a transcription reaction can be accurately determined as a function of measured pH. In addition, it is demonstrated that this method has significant value as a tool for achieving improved understanding of the effects of varying solution conditions on the dynamics of RNA transcription. Magnesium concentration was found to be a critical factor for efficient transcription. Below 5 mM free Mg2+ concentration, the transcription rate and the efficiency at which nucleoside triphosphates (NTPs) are incorporated are greatly reduced. While inorganic pyrophosphate (PPi), a byproduct of the reaction, was found to directly inhibit the rate of transcription, its detrimental effects on transcription were determined to be primarily due to sequestering of magnesium. The PPi forms a precipitate with magnesium which was determined to have a molar composition of 2:1 of Mg:PPi. Transcription rate and efficiency of NTP incorporation are also reduced with increasing ionic strength. It is shown that these reductions can be partially alleviated by replacing chloride with acetate anions.</description><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Chemical Precipitation</subject><subject>Diverse techniques</subject><subject>DNA</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>Hydrogen-Ion Concentration</subject><subject>Kinetics</subject><subject>Magnesium - administration & dosage</subject><subject>Magnesium - pharmacology</subject><subject>Methods. Procedures. Technologies</subject><subject>Miscellaneous</subject><subject>Molecular and cellular biology</subject><subject>Nucleotides - metabolism</subject><subject>Osmolar Concentration</subject><subject>Phosphates - metabolism</subject><subject>RNA - genetics</subject><subject>RNA - metabolism</subject><subject>Solutions</subject><subject>Synthetic digonucleotides and genes. Sequencing</subject><subject>Templates, Genetic</subject><subject>Transcription, Genetic</subject><issn>8756-7938</issn><issn>1520-6033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAURYMo4zi68AcIXYjgopqvJs1yGPxkUBBdlyRNIZI2naQV5t-bccpsXb0H97wL7wBwieAdghjdq15wCAXtj8AcFRjmDBJyDOYlL1jOBSlPwVmM3xDCEjI8AzNBEUEEz8Hrsu-d1XKwvst8k0Xvxr_dbEbrrAp2bDPZSbeNNmaDz2yX_dgh-OzjbZkNQXZRB9vvTs7BSSNdNBfTXICvx4fP1XO-fn96WS3XuaaUDLmgTGhW11oKjhSFXCCjCs6NMkoTjoysMURCFo3EQgqTHmNQoUZgXUJCGVmAm31vH_xmNHGoWhu1cU52xo-x4oKWjCcB_4GI4dQtRAJv96AOPsZgmqoPtpVhWyFY7QRXB8GJvZpKR9Wa-kBORlN-PeUyaumaZEjbeMAwwgVJf_wCesOCoA</recordid><startdate>19971101</startdate><enddate>19971101</enddate><creator>KERN, J. A</creator><creator>DAVIS, R. 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H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-9469c6ddca971b40791eb577ebebc371ead2019a5fa29a9e70060b1f92c803463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Chemical Precipitation</topic><topic>Diverse techniques</topic><topic>DNA</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>Hydrogen-Ion Concentration</topic><topic>Kinetics</topic><topic>Magnesium - administration & dosage</topic><topic>Magnesium - pharmacology</topic><topic>Methods. Procedures. Technologies</topic><topic>Miscellaneous</topic><topic>Molecular and cellular biology</topic><topic>Nucleotides - metabolism</topic><topic>Osmolar Concentration</topic><topic>Phosphates - metabolism</topic><topic>RNA - genetics</topic><topic>RNA - metabolism</topic><topic>Solutions</topic><topic>Synthetic digonucleotides and genes. Sequencing</topic><topic>Templates, Genetic</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KERN, J. A</creatorcontrib><creatorcontrib>DAVIS, R. H</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology progress</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KERN, J. A</au><au>DAVIS, R. H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of solution equilibrium analysis to in vitro RNA transcription</atitle><jtitle>Biotechnology progress</jtitle><addtitle>Biotechnol Prog</addtitle><date>1997-11-01</date><risdate>1997</risdate><volume>13</volume><issue>6</issue><spage>747</spage><epage>756</epage><pages>747-756</pages><issn>8756-7938</issn><eissn>1520-6033</eissn><coden>BIPRET</coden><abstract>Solution equilibrium analysis of in vitro RNA transcription has been applied to examine changes in pH, free magnesium concentration, and concentrations of all chemical ionization species as a transcription reaction proceeds. With this method, the progress of a transcription reaction can be accurately determined as a function of measured pH. In addition, it is demonstrated that this method has significant value as a tool for achieving improved understanding of the effects of varying solution conditions on the dynamics of RNA transcription. Magnesium concentration was found to be a critical factor for efficient transcription. Below 5 mM free Mg2+ concentration, the transcription rate and the efficiency at which nucleoside triphosphates (NTPs) are incorporated are greatly reduced. While inorganic pyrophosphate (PPi), a byproduct of the reaction, was found to directly inhibit the rate of transcription, its detrimental effects on transcription were determined to be primarily due to sequestering of magnesium. The PPi forms a precipitate with magnesium which was determined to have a molar composition of 2:1 of Mg:PPi. Transcription rate and efficiency of NTP incorporation are also reduced with increasing ionic strength. It is shown that these reductions can be partially alleviated by replacing chloride with acetate anions.</abstract><cop>Washington, DC</cop><cop>New York, NY</cop><pub>American Chemical Society</pub><pmid>9413132</pmid><doi>10.1021/bp970094p</doi><tpages>10</tpages></addata></record> |
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subjects | Base Sequence Biological and medical sciences Biotechnology Chemical Precipitation Diverse techniques DNA Fundamental and applied biological sciences. Psychology Genetic engineering Genetic technics Hydrogen-Ion Concentration Kinetics Magnesium - administration & dosage Magnesium - pharmacology Methods. Procedures. Technologies Miscellaneous Molecular and cellular biology Nucleotides - metabolism Osmolar Concentration Phosphates - metabolism RNA - genetics RNA - metabolism Solutions Synthetic digonucleotides and genes. Sequencing Templates, Genetic Transcription, Genetic |
title | Application of solution equilibrium analysis to in vitro RNA transcription |
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