Cloning of Xanthomonas DNA that expresses d-xylose catabolic enzymes
A gene bank of the d-xylose utilizing, cellulolytic Xanthomonas (XA1-1) DNA, inserted into the Hind III site of pKT230, was screened for clones which encoded d-xylose isomerase. One clone (pND70) was identified which complemented d-xylose isomerase negative mutants of Escherichia coli and this clone...
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Veröffentlicht in: | Journal of biotechnology 1987, Vol.6 (2), p.159-165 |
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creator | Liu, Chun-Qiang Lucas, Rachel J. Daly, Jan M. Rickard, Pamela A.D. Dunn, Noel W. |
description | A gene bank of the
d-xylose utilizing, cellulolytic
Xanthomonas (XA1-1) DNA, inserted into the
Hind III site of pKT230, was screened for clones which encoded
d-xylose isomerase. One clone (pND70) was identified which complemented
d-xylose isomerase negative mutants of
Escherichia coli and this clone contained an insert of XA1-1 DNA of approximately 15 kb. Enzyme assays showed that pND70 appeared to encode
d-xylose permease, and xylulose kinase in addition to
d-xylose isomerase. Specific activities of all 3 enzymes from
E. coli JA200 (pND70) grown in
d-xylose were double those detected in XA1-1 when also grown on
d-xylose. |
doi_str_mv | 10.1016/0168-1656(87)90053-8 |
format | Article |
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d-xylose utilizing, cellulolytic
Xanthomonas (XA1-1) DNA, inserted into the
Hind III site of pKT230, was screened for clones which encoded
d-xylose isomerase. One clone (pND70) was identified which complemented
d-xylose isomerase negative mutants of
Escherichia coli and this clone contained an insert of XA1-1 DNA of approximately 15 kb. Enzyme assays showed that pND70 appeared to encode
d-xylose permease, and xylulose kinase in addition to
d-xylose isomerase. Specific activities of all 3 enzymes from
E. coli JA200 (pND70) grown in
d-xylose were double those detected in XA1-1 when also grown on
d-xylose.</description><identifier>ISSN: 0168-1656</identifier><identifier>EISSN: 1873-4863</identifier><identifier>DOI: 10.1016/0168-1656(87)90053-8</identifier><identifier>CODEN: JBITD4</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Biological and medical sciences ; Biotechnology ; Cloning ; d-Xylose isomerase ; Escherichia coli ; Expression ; Fundamental and applied biological sciences. Psychology ; genes ; Genetic engineering ; Genetic technics ; Methods. Procedures. Technologies ; Molecular cloning ; Xanthomonas ; Xanthomonas albilineans ; xylose isomerase ; xylose permease ; xylulose kinase</subject><ispartof>Journal of biotechnology, 1987, Vol.6 (2), p.159-165</ispartof><rights>1987</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c366t-52f903f6e7556cb9d937371a69766d2f7b64a09eb02b3900432ef39899e996543</citedby><cites>FETCH-LOGICAL-c366t-52f903f6e7556cb9d937371a69766d2f7b64a09eb02b3900432ef39899e996543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0168165687900538$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,4010,27900,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7562371$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Chun-Qiang</creatorcontrib><creatorcontrib>Lucas, Rachel J.</creatorcontrib><creatorcontrib>Daly, Jan M.</creatorcontrib><creatorcontrib>Rickard, Pamela A.D.</creatorcontrib><creatorcontrib>Dunn, Noel W.</creatorcontrib><title>Cloning of Xanthomonas DNA that expresses d-xylose catabolic enzymes</title><title>Journal of biotechnology</title><description>A gene bank of the
d-xylose utilizing, cellulolytic
Xanthomonas (XA1-1) DNA, inserted into the
Hind III site of pKT230, was screened for clones which encoded
d-xylose isomerase. One clone (pND70) was identified which complemented
d-xylose isomerase negative mutants of
Escherichia coli and this clone contained an insert of XA1-1 DNA of approximately 15 kb. Enzyme assays showed that pND70 appeared to encode
d-xylose permease, and xylulose kinase in addition to
d-xylose isomerase. Specific activities of all 3 enzymes from
E. coli JA200 (pND70) grown in
d-xylose were double those detected in XA1-1 when also grown on
d-xylose.</description><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cloning</subject><subject>d-Xylose isomerase</subject><subject>Escherichia coli</subject><subject>Expression</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>genes</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>Methods. Procedures. Technologies</subject><subject>Molecular cloning</subject><subject>Xanthomonas</subject><subject>Xanthomonas albilineans</subject><subject>xylose isomerase</subject><subject>xylose permease</subject><subject>xylulose kinase</subject><issn>0168-1656</issn><issn>1873-4863</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNp9kD9PwzAQxS0EEqXwDRgyIARDwI4TO16QqpZ_UgULSGyW45ypURoXX4paPj0pRR0ZTrf83rt7j5BTRq8YZeK6nzJlohAXpbxUlBY8LffIgJWSp3kp-D4Z7JBDcoT4QSnNVcEGZDJuQuvb9yS45M203SzMQ2swmTyNkm5mugRWiwiIgEmdrtZNQEis6UwVGm8TaL_Xc8BjcuBMg3Dyt4fk9e72ZfyQTp_vH8ejaWq5EF1aZE5R7gTIohC2UrXikktmhJJC1JmTlcgNVVDRrOJ9jJxn4LgqlQKlRJHzITnf-i5i-FwCdnru0ULTmBbCEjXLVa6yjPVgvgVtDIgRnF5EPzdxrRnVm8r0pg-96UOXUv9Wpstedvbnb9CaxkXTWo87rSxE1v_bYzdbDPqsXx6iRuuhtVD7CLbTdfD_3_kBAfV96w</recordid><startdate>1987</startdate><enddate>1987</enddate><creator>Liu, Chun-Qiang</creator><creator>Lucas, Rachel J.</creator><creator>Daly, Jan M.</creator><creator>Rickard, Pamela A.D.</creator><creator>Dunn, Noel W.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>1987</creationdate><title>Cloning of Xanthomonas DNA that expresses d-xylose catabolic enzymes</title><author>Liu, Chun-Qiang ; Lucas, Rachel J. ; Daly, Jan M. ; Rickard, Pamela A.D. ; Dunn, Noel W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c366t-52f903f6e7556cb9d937371a69766d2f7b64a09eb02b3900432ef39899e996543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cloning</topic><topic>d-Xylose isomerase</topic><topic>Escherichia coli</topic><topic>Expression</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>genes</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>Methods. Procedures. Technologies</topic><topic>Molecular cloning</topic><topic>Xanthomonas</topic><topic>Xanthomonas albilineans</topic><topic>xylose isomerase</topic><topic>xylose permease</topic><topic>xylulose kinase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Chun-Qiang</creatorcontrib><creatorcontrib>Lucas, Rachel J.</creatorcontrib><creatorcontrib>Daly, Jan M.</creatorcontrib><creatorcontrib>Rickard, Pamela A.D.</creatorcontrib><creatorcontrib>Dunn, Noel W.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids 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>Genetics Abstracts</collection><jtitle>Journal of biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Chun-Qiang</au><au>Lucas, Rachel J.</au><au>Daly, Jan M.</au><au>Rickard, Pamela A.D.</au><au>Dunn, Noel W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cloning of Xanthomonas DNA that expresses d-xylose catabolic enzymes</atitle><jtitle>Journal of biotechnology</jtitle><date>1987</date><risdate>1987</risdate><volume>6</volume><issue>2</issue><spage>159</spage><epage>165</epage><pages>159-165</pages><issn>0168-1656</issn><eissn>1873-4863</eissn><coden>JBITD4</coden><abstract>A gene bank of the
d-xylose utilizing, cellulolytic
Xanthomonas (XA1-1) DNA, inserted into the
Hind III site of pKT230, was screened for clones which encoded
d-xylose isomerase. One clone (pND70) was identified which complemented
d-xylose isomerase negative mutants of
Escherichia coli and this clone contained an insert of XA1-1 DNA of approximately 15 kb. Enzyme assays showed that pND70 appeared to encode
d-xylose permease, and xylulose kinase in addition to
d-xylose isomerase. Specific activities of all 3 enzymes from
E. coli JA200 (pND70) grown in
d-xylose were double those detected in XA1-1 when also grown on
d-xylose.</abstract><cop>Lausanne</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><doi>10.1016/0168-1656(87)90053-8</doi><tpages>7</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals |
subjects | Biological and medical sciences Biotechnology Cloning d-Xylose isomerase Escherichia coli Expression Fundamental and applied biological sciences. Psychology genes Genetic engineering Genetic technics Methods. Procedures. Technologies Molecular cloning Xanthomonas Xanthomonas albilineans xylose isomerase xylose permease xylulose kinase |
title | Cloning of Xanthomonas DNA that expresses d-xylose catabolic enzymes |
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