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. 1992 Sep;174(17):5604–5608. doi: 10.1128/jb.174.17.5604-5608.1992

Cloning, characterization, and DNA base sequence of the high-level streptomycin resistance gene strA1 of Haemophilus influenzae Rd.

J H Stuy 1, R B Walter 1
PMCID: PMC206505  PMID: 1512195

Abstract

The high-level streptomycin resistance strA1 gene of Haemophilus influenzae Rd was cloned in plasmid pAT4 as a 2.1-kbp EcoRI insert. It was later replaced in pAT4 by the wild-type strA+ gene. Plasmid pAT4 carrying the strA+ gene is highly unstable and renders chromosomally resistant recipients sensitive to streptomycin. The strA+ gene and the instability factor both reside on a 500-base HindIII-EcoRI subfragment. The two biological activities are also expressed in Escherichia coli. Both wild-type (strA+) and mutant (strA1) genes were sequenced. They show considerable nucleotide homology with the E. coli strA+ gene and its product.

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Selected References

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  1. Balganesh M., Arrigoni L., Setlow J. K. Plasmid-to-chromosome gene transfer in Haemophilus influenza during growth. J Bacteriol. 1986 Oct;168(1):458–459. doi: 10.1128/jb.168.1.458-459.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barcak G. J., Tomb J. F., Laufer C. S., Smith H. O. Two Haemophilus influenzae Rd genes that complement the recA-like mutation rec-1. J Bacteriol. 1989 May;171(5):2451–2457. doi: 10.1128/jb.171.5.2451-2457.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Barnhart B. J., Cox S. H. Radiation-sensitive and radiation-resistant mutants of Haemophilus influenzae. J Bacteriol. 1968 Jul;96(1):280–282. doi: 10.1128/jb.96.1.280-282.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bonny C., Montandon P. E., Marc-Martin S., Stutz E. Analysis of streptomycin-resistance of Escherichia coli mutants. Biochim Biophys Acta. 1991 Jun 13;1089(2):213–219. doi: 10.1016/0167-4781(91)90010-j. [DOI] [PubMed] [Google Scholar]
  5. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Goodgal S. H., Mitchell M. A. Sequence and uptake specificity of cloned sonicated fragments of Haemophilus influenzae DNA. J Bacteriol. 1990 Oct;172(10):5924–5928. doi: 10.1128/jb.172.10.5924-5928.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. LEDERBERG J. Streptomycin resistance; a genetically recessive mutation. J Bacteriol. 1951 May;61(5):549–550. doi: 10.1128/jb.61.5.549-550.1951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Leclerc D., Melançon P., Brakier-Gingras L. Mutations in the 915 region of Escherichia coli 16S ribosomal RNA reduce the binding of streptomycin to the ribosome. Nucleic Acids Res. 1991 Jul 25;19(14):3973–3977. doi: 10.1093/nar/19.14.3973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lindahl L., Zengel J. M. Ribosomal genes in Escherichia coli. Annu Rev Genet. 1986;20:297–326. doi: 10.1146/annurev.ge.20.120186.001501. [DOI] [PubMed] [Google Scholar]
  10. Post L. E., Nomura M. DNA sequences from the str operon of Escherichia coli. J Biol Chem. 1980 May 25;255(10):4660–4666. [PubMed] [Google Scholar]
  11. STUY J. H. Transformability of Haemophilus influenzae. J Gen Microbiol. 1962 Nov;29:537–549. doi: 10.1099/00221287-29-3-537. [DOI] [PubMed] [Google Scholar]
  12. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Setlow J. K., Brown D. C., Boling M. E., Mattingly A., Gordon M. P. Repair of deoxyribonucleic acid in Haemophilus influenzae. I. X-ray sensitivity of ultraviolet-sensitive mutants and their behavior as hosts to ultraviolet-irradiated bacteriophage and transforming deoxyribonucleic acid. J Bacteriol. 1968 Feb;95(2):546–558. doi: 10.1128/jb.95.2.546-558.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Setlow J. K., Spikes D., Griffin K. Characterization of the rec-1 gene of Haemophilus influenzae and behavior of the gene in Escherichia coli. J Bacteriol. 1988 Sep;170(9):3876–3881. doi: 10.1128/jb.170.9.3876-3881.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Sisco K. L., Smith H. O. Sequence-specific DNA uptake in Haemophilus transformation. Proc Natl Acad Sci U S A. 1979 Feb;76(2):972–976. doi: 10.1073/pnas.76.2.972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Stuy J. H. Cloning and characterization of the Haemophilus influenzae Rd rec-1+ gene. J Bacteriol. 1989 Aug;171(8):4395–4401. doi: 10.1128/jb.171.8.4395-4401.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Stuy J. H. On the nature of nontypable Haemophilus influenzae. Antonie Van Leeuwenhoek. 1978;44(3-4):367–376. doi: 10.1007/BF00394313. [DOI] [PubMed] [Google Scholar]
  18. Stuy J. H. Plasmid transfer in Haemophilus influenzae. J Bacteriol. 1979 Aug;139(2):520–529. doi: 10.1128/jb.139.2.520-529.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Stuy J. H., Walter R. B. Effect of glycerol on plasmid transfer in genetically competent Haemophilus influenzae. Mol Gen Genet. 1986 May;203(2):296–299. doi: 10.1007/BF00333969. [DOI] [PubMed] [Google Scholar]
  20. Stuy J. H., Walter R. B. Homology-facilitated plasmid transfer in Haemophilus influenzae. Mol Gen Genet. 1986 May;203(2):288–295. doi: 10.1007/BF00333968. [DOI] [PubMed] [Google Scholar]
  21. Vieira J., Messing J. The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers. Gene. 1982 Oct;19(3):259–268. doi: 10.1016/0378-1119(82)90015-4. [DOI] [PubMed] [Google Scholar]

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