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Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression.

Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression. Research Abstract Details 

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  • Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression. Abstract Text:

    wei wangWei Wang,larry reitzerLarry Reitzer,david a raskoDavid A Rasko,melanie m pearsonMelanie M Pearson,robert j blickRobert J Blick,cassie laurenceCassie Laurence,eric j hansenEric J Hansen,

    The nucleotide sequence from the genome of Moraxella catarrhalis ATCC 43617 was annotated and used both to assess the metabolic capabilities and limitations of this bacterium and to design probes for a DNA microarray. An absence of gene products for utilization of exogenous carbohydrates was noteworthy and could be correlated with published phenotypic data. Gene products necessary for aerobic energy generation were present, as were a few gene products generally ascribed to anaerobic systems. Enzymes for synthesis of all amino acids except proline and arginine were present. M. catarrhalis DNA microarrays containing 70-mer oligonucleotide probes were designed from the genome-derived nucleotide sequence data. Analysis of total RNA extracted from M. catarrhalis ATCC 43617 cells grown under iron-replete and iron-restricted conditions was used to establish the utility of these DNA microarrays. These DNA microarrays were then used to analyze total RNA from M. catarrhalis cells grown in a continuous-flow biofilm system and in the planktonic state. The genes whose expression was most dramatically increased by growth in the biofilm state included those encoding a nitrate reductase, a nitrite reductase, and a nitric oxide reductase. Real-time reverse transcriptase PCR analysis was used to validate these DNA microarray results. These results indicate that growth of M. catarrhalis in a biofilm results in increased expression of gene products which can function not only in energy generation but also in resisting certain elements of the innate immune response.

    Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression. Publishing Authors By Initials

    w wangW Wang,l reitzerL Reitzer,da raskoDA Rasko,mm pearsonMM Pearson,rj blickRJ Blick,c laurenceC Laurence,ej hansenEJ Hansen,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Infection and immunity

    VOLUME: 75

    Page Numbers: 4959-71

    Journal Abbreviation: Infect. Immun.

    ISSN: 0019-9567

    DAY: 9

    MONTH: 07

    YEAR: 2007

    Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 246127

    Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression. Keywords Mesh Terms:

    KEYWORDS: Reverse Transcriptase Polymerase Chain R

    MESH TERMS: isolation & purification

    Chemical & Substance for Abstract: Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression. Information

    Substance Name: Iron

    Registry Number: 7439-89-6

    Grant and Affiliation Information for Metabolic analysis of Moraxella catarrhalis and the effect of selected in vitro growth conditions on global gene expression.

    AFFILIATION: Department of Microbiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9048, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAID

    GRANT: AI36344

    ACRONYM: AI

    MEDLINETA: Infect Immun

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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