Molecular cloning, sequencing, and expression of omp-40, the gene coding for the major outer membrane protein from the acidophilic bacterium Thiobacillus ferrooxidans

• Published in: Applied and environmental microbiology Vol. 66; no. 6; pp. 2318 - 2324
• Main Authors: GUILIANI, N, JEREZ, C. A
• Format: Journal Article
• Language: English
• Published: Washington, DC American Society for Microbiology 01.06.2000
• Subjects: Amino Acid Sequence; Bacteria; Bacterial Outer Membrane Proteins - chemistry; Bacterial Outer Membrane Proteins - genetics; Bacterial Outer Membrane Proteins - metabolism; Base Sequence; Biological and medical sciences; Biology of microorganisms of confirmed or potential industrial interest; Biotechnology; Cloning; Cloning, Molecular; Escherichia coli - genetics; Escherichia coli - metabolism; Fundamental and applied biological sciences. Psychology; Genetics; Genetics and Molecular Biology; Microbiology; Mission oriented research; Models, Molecular; Molecular Sequence Data; omp40 gene; Omp40 protein; Protein Folding; Proteins; Sequence Analysis, DNA; Solubility; Thiobacillus - genetics; Thiobacillus - metabolism; Thiobacillus ferrooxidans; Transcription, Genetic; Acidophily; Porin; Purification; Nucleotide sequence; Industrial application; Escherichia coli; Homology; Bacterial leaching; Gene expression; External membrane; Protein; Bacteria; Recombinant protein; Thiobacillus ferrooxidans; Enterobacteriaceae
• ISSN: 0099-2240; 1098-5336
• DOI: 10.1128/AEM.66.6.2318-2324.2000

Thiobacillus ferrooxidans is one of the chemolithoautotrophic bacteria important in industrial biomining operations. Some of the surface components of this microorganism are probably involved in adaptation to their acidic environment and in bacterium-mineral interactions. We have isolated and characterized omp40, the gene coding for the major outer membrane protein from T. ferrooxidans. The deduced amino acid sequence of the Omp40 protein has 382 amino acids and a calculated molecular weight of 40,095.7. Omp40 forms an oligomeric structure of about 120 kDa that dissociates into the monomer (40 kDa) by heating in the presence of sodium dodecyl sulfate. The degree of identity of Omp40 amino acid sequence to porins from enterobacteria was only 22%. Nevertheless, multiple alignments of this sequence with those from several OmpC porins showed several important features conserved in the T. ferrooxidans surface protein, such as the approximate locations of 16 transmembrane beta strands, eight loops, including a large external L3 loop, and eight turns which allowed us to propose a putative 16-stranded beta-barrel porin structure for the protein. These results together with the previously known capacity of Omp40 to form ion channels in planar lipid bilayers strongly support its role as a porin in this chemolithoautotrophic acidophilic microorganism. Some characteristics of the Omp40 protein, such as the presence of a putative L3 loop with an estimated isoelectric point of 7.21 allow us to speculate that this can be the result of an adaptation of the acidophilic T. ferrooxidans to prevent free movement of protons across its outer membrane.