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Expression of the core antigen gene of hepatitis B virus (HBV) in Acetobacter methanolicus using broad-host-range vectors
Using the broad-host-range promoter probe vector pRS201 for cloning of phage Acm1 promoters, we established a convenient vector system for expression of heterologous genes in different Gram-negative bacteria. The usefulness of this system was demonstrated by expression of the HBV core gene in Acetob...
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Published in: | Applied microbiology and biotechnology 1991-08, Vol.35 (5), p.631-637 |
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container_title | Applied microbiology and biotechnology |
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creator | SCHRODER, R MAASSEN, A LIPPOLDT, A BORNER, T BON BAEHR, R DOBROWOLSKI, P |
description | Using the broad-host-range promoter probe vector pRS201 for cloning of phage Acm1 promoters, we established a convenient vector system for expression of heterologous genes in different Gram-negative bacteria. The usefulness of this system was demonstrated by expression of the HBV core gene in Acetobacter methanolicus. Plasmids carrying the HBV core gene downstream of different Acm1-phage promoters were transferred to A. methanolicus, a new potential host for recombinant DNA expression. Using enzyme immunoassay and immunoblot techniques, the amount and composition of core antigen produced in A. methanolicus were compared with that derived from Escherichia coli. The expression of immunoreactive core antigen in A. methanolicus exceeds by sevenfold that in E. coli using an expression system with tandemly arranged promoters. Morphological observations by electron microscopy show that the HBV core gene products isolated from both hosts are assembled into regular spherical particles with a diameter of about 28 nm that are comparable to original viral nucleocapsids. |
doi_str_mv | 10.1007/BF00169628 |
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The usefulness of this system was demonstrated by expression of the HBV core gene in Acetobacter methanolicus. Plasmids carrying the HBV core gene downstream of different Acm1-phage promoters were transferred to A. methanolicus, a new potential host for recombinant DNA expression. Using enzyme immunoassay and immunoblot techniques, the amount and composition of core antigen produced in A. methanolicus were compared with that derived from Escherichia coli. The expression of immunoreactive core antigen in A. methanolicus exceeds by sevenfold that in E. coli using an expression system with tandemly arranged promoters. Morphological observations by electron microscopy show that the HBV core gene products isolated from both hosts are assembled into regular spherical particles with a diameter of about 28 nm that are comparable to original viral nucleocapsids.</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/BF00169628</identifier><identifier>PMID: 1367579</identifier><identifier>CODEN: AMBIDG</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Acetobacter - genetics ; Amino Acid Sequence ; Base Sequence ; Biological and medical sciences ; Biotechnology ; Cloning, Molecular - methods ; DNA, Recombinant ; Escherichia coli - genetics ; Fundamental and applied biological sciences. Psychology ; Genes, Viral ; Genetic engineering ; Genetic Markers ; Genetic technics ; Genetic Vectors ; Hepatitis B Core Antigens - genetics ; hepatitis B virus ; Hepatitis B virus - genetics ; Methods. Procedures. Technologies ; Modification of gene expression level ; Molecular Sequence Data ; Oligodeoxyribonucleotides ; Plasmids ; Restriction Mapping</subject><ispartof>Applied microbiology and biotechnology, 1991-08, Vol.35 (5), p.631-637</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c378t-d548a8efaebd7c9de9185d43854d07b9923315b239596806e41276a2bfd255db3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5034275$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1367579$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SCHRODER, R</creatorcontrib><creatorcontrib>MAASSEN, A</creatorcontrib><creatorcontrib>LIPPOLDT, A</creatorcontrib><creatorcontrib>BORNER, T</creatorcontrib><creatorcontrib>BON BAEHR, R</creatorcontrib><creatorcontrib>DOBROWOLSKI, P</creatorcontrib><title>Expression of the core antigen gene of hepatitis B virus (HBV) in Acetobacter methanolicus using broad-host-range vectors</title><title>Applied microbiology and biotechnology</title><addtitle>Appl Microbiol Biotechnol</addtitle><description>Using the broad-host-range promoter probe vector pRS201 for cloning of phage Acm1 promoters, we established a convenient vector system for expression of heterologous genes in different Gram-negative bacteria. The usefulness of this system was demonstrated by expression of the HBV core gene in Acetobacter methanolicus. Plasmids carrying the HBV core gene downstream of different Acm1-phage promoters were transferred to A. methanolicus, a new potential host for recombinant DNA expression. Using enzyme immunoassay and immunoblot techniques, the amount and composition of core antigen produced in A. methanolicus were compared with that derived from Escherichia coli. The expression of immunoreactive core antigen in A. methanolicus exceeds by sevenfold that in E. coli using an expression system with tandemly arranged promoters. Morphological observations by electron microscopy show that the HBV core gene products isolated from both hosts are assembled into regular spherical particles with a diameter of about 28 nm that are comparable to original viral nucleocapsids.</description><subject>Acetobacter - genetics</subject><subject>Amino Acid Sequence</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cloning, Molecular - methods</subject><subject>DNA, Recombinant</subject><subject>Escherichia coli - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Viral</subject><subject>Genetic engineering</subject><subject>Genetic Markers</subject><subject>Genetic technics</subject><subject>Genetic Vectors</subject><subject>Hepatitis B Core Antigens - genetics</subject><subject>hepatitis B virus</subject><subject>Hepatitis B virus - genetics</subject><subject>Methods. Procedures. 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Psychology</topic><topic>Genes, Viral</topic><topic>Genetic engineering</topic><topic>Genetic Markers</topic><topic>Genetic technics</topic><topic>Genetic Vectors</topic><topic>Hepatitis B Core Antigens - genetics</topic><topic>hepatitis B virus</topic><topic>Hepatitis B virus - genetics</topic><topic>Methods. Procedures. Technologies</topic><topic>Modification of gene expression level</topic><topic>Molecular Sequence Data</topic><topic>Oligodeoxyribonucleotides</topic><topic>Plasmids</topic><topic>Restriction Mapping</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SCHRODER, R</creatorcontrib><creatorcontrib>MAASSEN, A</creatorcontrib><creatorcontrib>LIPPOLDT, A</creatorcontrib><creatorcontrib>BORNER, T</creatorcontrib><creatorcontrib>BON BAEHR, R</creatorcontrib><creatorcontrib>DOBROWOLSKI, P</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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Applied microbiology and biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SCHRODER, R</au><au>MAASSEN, A</au><au>LIPPOLDT, A</au><au>BORNER, T</au><au>BON BAEHR, R</au><au>DOBROWOLSKI, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of the core antigen gene of hepatitis B virus (HBV) in Acetobacter methanolicus using broad-host-range vectors</atitle><jtitle>Applied microbiology and biotechnology</jtitle><addtitle>Appl Microbiol Biotechnol</addtitle><date>1991-08-01</date><risdate>1991</risdate><volume>35</volume><issue>5</issue><spage>631</spage><epage>637</epage><pages>631-637</pages><issn>0175-7598</issn><eissn>1432-0614</eissn><coden>AMBIDG</coden><abstract>Using the broad-host-range promoter probe vector pRS201 for cloning of phage Acm1 promoters, we established a convenient vector system for expression of heterologous genes in different Gram-negative bacteria. The usefulness of this system was demonstrated by expression of the HBV core gene in Acetobacter methanolicus. Plasmids carrying the HBV core gene downstream of different Acm1-phage promoters were transferred to A. methanolicus, a new potential host for recombinant DNA expression. Using enzyme immunoassay and immunoblot techniques, the amount and composition of core antigen produced in A. methanolicus were compared with that derived from Escherichia coli. The expression of immunoreactive core antigen in A. methanolicus exceeds by sevenfold that in E. coli using an expression system with tandemly arranged promoters. Morphological observations by electron microscopy show that the HBV core gene products isolated from both hosts are assembled into regular spherical particles with a diameter of about 28 nm that are comparable to original viral nucleocapsids.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>1367579</pmid><doi>10.1007/BF00169628</doi><tpages>7</tpages></addata></record> |
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subjects | Acetobacter - genetics Amino Acid Sequence Base Sequence Biological and medical sciences Biotechnology Cloning, Molecular - methods DNA, Recombinant Escherichia coli - genetics Fundamental and applied biological sciences. Psychology Genes, Viral Genetic engineering Genetic Markers Genetic technics Genetic Vectors Hepatitis B Core Antigens - genetics hepatitis B virus Hepatitis B virus - genetics Methods. Procedures. Technologies Modification of gene expression level Molecular Sequence Data Oligodeoxyribonucleotides Plasmids Restriction Mapping |
title | Expression of the core antigen gene of hepatitis B virus (HBV) in Acetobacter methanolicus using broad-host-range vectors |
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