Tagging exported proteins using Escherichia coli alkaline phosphatase gene fusions (Q45039719)

8 December 2017

Tagging exported proteins using Escherichia coli alkaline phosphatase gene fusions (English)

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8 December 2017

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Manoil C

1

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PubMed ID

11036633

8 December 2017

language of work or name

English

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publication date

1 January 2000

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8 December 2017

Methods in Enzymology

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8 December 2017

326

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8 December 2017

35-47

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Escherichia coli alkaline phosphatase fails to acquire disulfide bonds when retained in the cytoplasm

8 December 2017

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The topological analysis of integral cytoplasmic membrane proteins

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Insertion of in-frame sequence tags into proteins using transposons.

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Identification of bacterial cell-surface virulence determinants with TnphoA.

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TnphoA and TnphoA' elements for making and switching fusions for study of transcription, translation, and cell surface localization

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Construction of transposon Tn3phoA: its application in defining the membrane topology of the Agrobacterium tumefaciens DNA transfer proteins

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Construction of an alkaline phosphatase fusion-generating transposon, mTn10phoA.

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A simple screen for permissive sites in proteins: analysis of Escherichia coli lac permease.

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Allelic exchange in Escherichia coli using the Bacillus subtilis sacB gene and a temperature-sensitive pSC101 replicon

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Transposon vectors containing non-antibiotic resistance selection markers for cloning and stable chromosomal insertion of foreign genes in gram-negative bacteria

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A novel suicide vector and its use in construction of insertion mutations: osmoregulation of outer membrane proteins and virulence determinants in Vibrio cholerae requires toxR

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A mutational analysis of the bacteriophage P1 recombinase Cre.

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Analysis of the regulation of Escherichia coli alkaline phosphatase synthesis using deletions and φ80 transducing phages

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Escherichia coli alkaline phosphatase localized to the cytoplasm slowly acquires enzymatic activity in cells whose growth has been suspended: a caution for gene fusion studies

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Alkaline phosphatase fusions: sensors of subcellular location

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The LysR homolog LrhA promotes RpoS degradation by modulating activity of the response regulator sprE.

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Use of phoA fusions to study the topology of the Escherichia coli inner membrane protein leader peptidase

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Identifiers

DOI

1 reference

8 December 2017

1 reference

PubMed ID

11036633