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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Lincomycin resistance gene lnu(D) in Streptococcus uberis

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Συγγραφέας
Petinaki, E.; Guérin-Faublée, V.; Pichereau, V.; Villers, C.; Achard, A.; Malbruny, B.; Leclercq, R.
Ημερομηνία
2008
DOI
10.1128/AAC.01126-07
Λέξη-κλειδί
adenosine triphosphate
aminoglycoside nucleotidyltransferase
bacterial protein
clindamycin
erythromycin
gene product
lincomycin
lincosamide o nucleotidyltransferase
magnesium chloride
nucleotidyltransferase
pirlimycin
unclassified drug
adenylation
antibiotic resistance
antibiotic sensitivity
article
bacterial gene
bacterium isolation
catalysis
cattle disease
controlled study
Escherichia coli
gene sequence
genetic code
inu gene
lina gene
linan2 gene
lind gene
mass spectrometry
minimum inhibitory concentration
molecular cloning
nonhuman
nucleotide sequence
plasmid
priority journal
protein domain
sequence analysis
Streptococcus agalactiae
Streptococcus uberis
Amino Acid Sequence
Animals
Anti-Bacterial Agents
Bacterial Proteins
Cattle
Drug Resistance, Bacterial
Female
Mastitis, Bovine
Microbial Sensitivity Tests
Molecular Sequence Data
Nucleotidyltransferases
Sequence Analysis, DNA
Streptococcus
Εμφάνιση Μεταδεδομένων
Επιτομή
Streptococcus uberis UCN 42, isolated from a case of bovine mastitis, was intermediately resistant to lincomycin (MIC = 2 μg/ml) while remaining susceptible to clindamycin (MIC = 0.06 μg/ml) and erythromycin. A 1.1-kb SacI fragment was cloned from S. uberis UCN 42 total DNA on plasmid pUC 18 and introduced into Escherichia coli AG100A, where it conferred resistance to both clindamycin and lincomycin. The sequence analysis of the fragment showed the presence of a new gene, named lnu(D), that encoded a 164-amino-acid protein with 53% identity with Lnu(C) previously reported to occur in Streptococcus agalactiae:Crude lysates of E. coli AG100A containing the cloned lnu(D) gene inactivated lincomycin and clindamycin in the presence of ATP and MgCl 2. Mass spectrometry experiments demonstrated that the lnu(D) enzyme catalyzed adenylylation of clindamycin. A domain conserved in deduced sequences of lincosamide O-nucleotidyltransferases Lnu(A), Lnu(C), LinAN2, and Lin(D) and in the aminoglycoside nucleotidyltransferase ANT(2″) was identified. Copyright © 2008, American Society for Microbiology. All Rights Reserved.
URI
http://hdl.handle.net/11615/32176
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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