1983
DOI: 10.1038/nbt1183-784
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A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative Bacteria

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Cited by 6,657 publications
(2,725 citation statements)
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“…Colloidal chitin was prepared as described by Lingappa and Lockhood 16 . Mutagenesis of P. maltophila: Random Tn5 mutagenesis of P. maltophila PM-4 was carried out using E. coli S17-1(pSUP1021) following the procedure as described earlier 17,18 .…”
Section: Methodsmentioning
confidence: 99%
“…Colloidal chitin was prepared as described by Lingappa and Lockhood 16 . Mutagenesis of P. maltophila: Random Tn5 mutagenesis of P. maltophila PM-4 was carried out using E. coli S17-1(pSUP1021) following the procedure as described earlier 17,18 .…”
Section: Methodsmentioning
confidence: 99%
“…Escherichia coli TOP10 (Invitrogen, Carlsbad, CA) was used for general cloning and blue/white screening, and E. coli S17-1 [17] was used as a mobilizing strain for constructing mutants. The B. mallei mutant strains used in this study were derivatives of ATCC 23344, a highly pathogenic clinical isolate and type strain of the species [18][19][20].…”
Section: Bacterial Strains and Growth Conditionsmentioning
confidence: 99%
“…The Escherichia coil strains used were HB101 (Boyer and Roulland Dussoix, 1969) and SM10 (Simon et al, 1983). For plant transformation a novel Agrobacterium tumefaciens strain was constructed, that harbors the non-T-DNA portion of Ti plasmid pTiBo542 of the hypervirulent A. tumefaciens strain A281 (Hood et al, 1986).…”
Section: Bacterial Strains and Culturesmentioning
confidence: 99%