Evaluation of the hok/sok killer locus for enhanced plasmid stability

The effectiveness of the hok/sok plasmid stability locus and mechanism of cloned‐gene loss was evaluated in shake‐flask cultures. Addition of the hok/sok locus dramitically increasedapparent plasmid segregational stability to the hok/sok− control. In terms of the number of generations before 10%of t...

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Veröffentlicht in:Biotechnology and bioengineering 1994-10, Vol.44 (8), p.912-921
Hauptverfasser: Wu, Kuowei, Wood, Thomas K.
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description The effectiveness of the hok/sok plasmid stability locus and mechanism of cloned‐gene loss was evaluated in shake‐flask cultures. Addition of the hok/sok locus dramitically increasedapparent plasmid segregational stability to the hok/sok− control. In terms of the number of generations before 10%of the population became plasmid‐free, segregational stability was increased by 11‐ to 20‐fold in different media in the absence of induction of the cloned‐gene (hok/sok+ plasmid stable for over 200 generations in all media tested). With constant expression of β‐galactosidase in the absence of an tibiotic, the segregational stability of the plasmid containing hok/sok was incresed more than 17‐ to 30‐fold when β‐galactosidase was expressed at 7–15 wt % of total cell protein. Although the hok/sok system stabilized the plasmid well infour different media (Luria‐Bertani (LB), LB glucose, M9C Trp, and a representative fedbatch medium), the ability of hok/sok to maintain the plasmid with induction of the cloned gene decreased as the complexity of the media increased. This result is better interpreted in terms of the influence of cloned‐gene expression on plasmidmaintenance; plasmid segregational stability decreased linearly as specificβ‐galactosidase activity increased. © 1994 John Wiley & Sons, Inc.
doi_str_mv 10.1002/bit.260440807
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Addition of the hok/sok locus dramitically increasedapparent plasmid segregational stability to the hok/sok− control. In terms of the number of generations before 10%of the population became plasmid‐free, segregational stability was increased by 11‐ to 20‐fold in different media in the absence of induction of the cloned‐gene (hok/sok+ plasmid stable for over 200 generations in all media tested). With constant expression of β‐galactosidase in the absence of an tibiotic, the segregational stability of the plasmid containing hok/sok was incresed more than 17‐ to 30‐fold when β‐galactosidase was expressed at 7–15 wt % of total cell protein. Although the hok/sok system stabilized the plasmid well infour different media (Luria‐Bertani (LB), LB glucose, M9C Trp, and a representative fedbatch medium), the ability of hok/sok to maintain the plasmid with induction of the cloned gene decreased as the complexity of the media increased. This result is better interpreted in terms of the influence of cloned‐gene expression on plasmidmaintenance; plasmid segregational stability decreased linearly as specificβ‐galactosidase activity increased. © 1994 John Wiley &amp; Sons, Inc.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.260440807</identifier><identifier>PMID: 18618909</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Bacteriology ; Biological and medical sciences ; Biology of microorganisms of confirmed or potential industrial interest ; Biotechnology ; cloned gene ; Fundamental and applied biological sciences. 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Bioeng</addtitle><description>The effectiveness of the hok/sok plasmid stability locus and mechanism of cloned‐gene loss was evaluated in shake‐flask cultures. Addition of the hok/sok locus dramitically increasedapparent plasmid segregational stability to the hok/sok− control. In terms of the number of generations before 10%of the population became plasmid‐free, segregational stability was increased by 11‐ to 20‐fold in different media in the absence of induction of the cloned‐gene (hok/sok+ plasmid stable for over 200 generations in all media tested). With constant expression of β‐galactosidase in the absence of an tibiotic, the segregational stability of the plasmid containing hok/sok was incresed more than 17‐ to 30‐fold when β‐galactosidase was expressed at 7–15 wt % of total cell protein. Although the hok/sok system stabilized the plasmid well infour different media (Luria‐Bertani (LB), LB glucose, M9C Trp, and a representative fedbatch medium), the ability of hok/sok to maintain the plasmid with induction of the cloned gene decreased as the complexity of the media increased. This result is better interpreted in terms of the influence of cloned‐gene expression on plasmidmaintenance; plasmid segregational stability decreased linearly as specificβ‐galactosidase activity increased. © 1994 John Wiley &amp; Sons, Inc.</description><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Biology of microorganisms of confirmed or potential industrial interest</subject><subject>Biotechnology</subject><subject>cloned gene</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Genetics</topic><topic>hok/sok locus</topic><topic>Microbiology</topic><topic>Mission oriented research</topic><topic>plasmid stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Kuowei</creatorcontrib><creatorcontrib>Wood, Thomas K.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Kuowei</au><au>Wood, Thomas K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of the hok/sok killer locus for enhanced plasmid stability</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>1994-10</date><risdate>1994</risdate><volume>44</volume><issue>8</issue><spage>912</spage><epage>921</epage><pages>912-921</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>The effectiveness of the hok/sok plasmid stability locus and mechanism of cloned‐gene loss was evaluated in shake‐flask cultures. Addition of the hok/sok locus dramitically increasedapparent plasmid segregational stability to the hok/sok− control. In terms of the number of generations before 10%of the population became plasmid‐free, segregational stability was increased by 11‐ to 20‐fold in different media in the absence of induction of the cloned‐gene (hok/sok+ plasmid stable for over 200 generations in all media tested). With constant expression of β‐galactosidase in the absence of an tibiotic, the segregational stability of the plasmid containing hok/sok was incresed more than 17‐ to 30‐fold when β‐galactosidase was expressed at 7–15 wt % of total cell protein. Although the hok/sok system stabilized the plasmid well infour different media (Luria‐Bertani (LB), LB glucose, M9C Trp, and a representative fedbatch medium), the ability of hok/sok to maintain the plasmid with induction of the cloned gene decreased as the complexity of the media increased. This result is better interpreted in terms of the influence of cloned‐gene expression on plasmidmaintenance; plasmid segregational stability decreased linearly as specificβ‐galactosidase activity increased. © 1994 John Wiley &amp; Sons, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18618909</pmid><doi>10.1002/bit.260440807</doi><tpages>10</tpages></addata></record>
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subjects Bacteriology
Biological and medical sciences
Biology of microorganisms of confirmed or potential industrial interest
Biotechnology
cloned gene
Fundamental and applied biological sciences. Psychology
Genetics
hok/sok locus
Microbiology
Mission oriented research
plasmid stability
title Evaluation of the hok/sok killer locus for enhanced plasmid stability
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