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Recent "microbial" articles

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Overexpression, purification, and characterization of VanX, a D-, D-dipeptidase which is essential for vancomycin resistance in Enterococcus faecium BM4147
Z Wu, G D Wright, and C T Walsh
Biochemistry 34 (8), 2455-63 (28 Feb 1995)
 
Characterization of vanY, a DD-carboxypeptidase from vancomycin-resistant Enterococcus faecium BM4147
G D Wright et al.
Antimicrobial agents and chemotherapy 36 (7), 1514-8 (Jul 1992)
 
Purification and characterization of VanR and the cytosolic domain of VanS: a two-component regulatory system required for vancomycin resistance in Enterococcus faecium BM4147
G D Wright, T R Holman, and C T Walsh
Biochemistry 32 (19), 5057-63 (18 May 1993)
 
Bacterial resistance to vancomycin: overproduction, purification, and characterization of VanC2 from Enterococcus casseliflavus as a D-Ala-D-Ser ligase
I S Park, C H Lin, and C T Walsh
Proceedings of the National Academy of Sciences of the United States of America 94 (19), 10040-4 (16 Sep 1997)
 
Vancomycin derivatives that inhibit peptidoglycan biosynthesis without binding D-Ala-D-Ala
M Ge et al.
Science (New York, N.Y.) 284 (5413), 507-11 (16 Apr 1999)
 
Glycosyltransferase domain of penicillin-binding protein 2a from Streptococcus pneumoniae is membrane associated
A M di Guilmi et al.
Journal of bacteriology 181 (9), 2773-81 (May 1999)
 
Molecular basis for vancomycin resistance in Enterococcus faecium BM4147: biosynthesis of a depsipeptide peptidoglycan precursor by vancomycin resistance proteins VanH and VanA
T D Bugg et al.
Biochemistry 30 (43), 10408-15 (29 Oct 1991)
 
Identification of vancomycin resistance protein VanA as a D-alanine:D-alanine ligase of altered substrate specificity
T D Bugg et al.
Biochemistry 30 (8), 2017-21 (26 Feb 1991)
 
Overexpression of the thiostrepton-resistance gene from Streptomyces azureus in Escherichia coli and characterization of recognition sites of the 23S rRNA A1067 2'-methyltransferase in the guanosine triphosphatase center of 23S ribosomal RNA
A Bechthold and H G Floss
European journal of biochemistry / FEBS 224 (2), 431-7 (01 Sep 1994)
 
Microbial genotype-phenotype mapping by class association rule mining
Bioinformatics 24 (13), 1523 (2008)
Motivation: Microbial phenotypes are typically due to the concerted action of multiple gene functions, yet the presence of each gene may have only a weak correlation with the observed phenotype. Hence, it may be more appropriate to examine co-occurrence between sets of genes and a phenotype (multiple-to-one) instead of pairwise relations between a single gene and the phenotype. Here, we propose an efficient class association rule mining algorithm, NETCAR, in order to extract sets of COGs (clusters of orthologous groups of proteins) associated with a phenotype from COG phylogenetic profiles and a phenotype profile. NETCAR takes into account the phylogenetic co-occurrence graph between COGs to restrict hypothesis space, and uses mutual information to evaluate the biconditional relation. Results: We examined the mining capability of pairwise and multiple-to-one association by using NETCAR to extract COGs relevant to six microbial phenotypes (aerobic, anaerobic, facultative, endospore, motility and Gram negative) from 11 969 unique COG profiles across 155 prokaryotic organisms. With the same level of false discovery rate, multiple-to-one association can extract about 10 times more relevant COGs than one-to-one association. We also reveal various topologies of association networks among COGs (modules) from extracted multiple-to-one correlation rules relevant with the six phenotypes; including a well-connected network for motility, a star-shaped network for aerobic and intermediate topologies for the other phenotypes. NETCAR outperforms a standard CAR mining algorithm, CARAPRIORI, while requiring several orders of magnitude less computational time for extracting 3-COG sets. Availability: Source code of the Java implementation is available as Supplementary Material at the Bioinformatics online website, or upon request to the author.

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