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pubmed-article:8935658pubmed:dateCreated1996-12-31lld:pubmed
pubmed-article:8935658pubmed:abstractTextTwo plasmid cloning vectors (pULMJ55 and pULMJ95) were constructed for Brevibacterium lactofermentum using the origin of replication of the endogenous plasmid pBL1. Plasmid pULMJ55 is a replacement vector with transcriptional terminators from the B. lactofermentum trp operon flanking the BglII cloning sites. Religation of the BglII digested vector without insert creates a 376 bp perfect palindrome that is not tolerated in B. lactofermentum, giving positive selection for recombinant plasmids with inserts. Plasmid pULMJ95 contains the promoter-less alpha-amylase gene from Streptomyces griseus downstream of the trp terminator and is particularly suitable for the detection of promoters which are activated late during the growth phase. alpha-Amylase is secreted and its activity can be detected using simple plate tests.lld:pubmed
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pubmed-article:8935658pubmed:authorpubmed-author:MartínJ FJFlld:pubmed
pubmed-article:8935658pubmed:authorpubmed-author:GilJ AJAlld:pubmed
pubmed-article:8935658pubmed:authorpubmed-author:CadenasR FRFlld:pubmed
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pubmed-article:8935658pubmed:pagination63-8lld:pubmed
pubmed-article:8935658pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:8935658pubmed:year1996lld:pubmed
pubmed-article:8935658pubmed:articleTitleConstruction of new cloning vectors for Brevibacterium lactofermentum.lld:pubmed
pubmed-article:8935658pubmed:affiliationDepartamento de Ecología, Genética y Microbiología, Universidad de León, Spain.lld:pubmed
pubmed-article:8935658pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8935658pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed