4.2 Article

Transcriptional profiling of genes involved in n-hexadecane compounds assimilation in the hydrocarbon degrading Dietzia cinnamea P4 strain

Journal

BRAZILIAN JOURNAL OF MICROBIOLOGY
Volume 44, Issue 2, Pages 639-647

Publisher

SPRINGER
DOI: 10.1590/S1517-83822013000200044

Keywords

Dietzia cinnamea; n-hexadecane assimilation; alk genes; rubredoxin-alkane monooxygenase; real-time quantitative RT-PCR

Categories

Funding

  1. PETROBRAS
  2. CNPq

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The petroleum-derived degrading Dietzia cinnamea strain P4 recently had its genome sequenced and annotated. This allowed employing the data on genes that are involved in the degradation of n-alkanes. To examine the physiological behavior of strain P4 in the presence of n-alkanes, the strain was grown under varying conditions of pH and temperature. D. cinnamea P4 was able to grow at pH 7.0-9.0 and at temperatures ranging from 35 degrees C to 45 degrees C. Experiments of gene expression by real-time quantitative RT-PCR throughout the complete growth cycle clearly indicated the induction of the regulatory gene alkU (TetR family) during early growth. During the logarithmic phase, a large increase in transcriptional levels of a lipid transporter gene was noted. Also, the expression of a gene that encodes the protein fused rubredoxin-alkane monooxygenase was enhanced. Both genes are probably under the influence of the AlkU regulator.

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