Genome Structure ofBacillus cereustsu1 and Genes Involved in Cellulose Degradation and Poly-3-Hydroxybutyrate Synthesis
Autor: | Parthasarathy Ranganathan, Koen Vercruysse, Theodore W. Thannhauser, Suping Zhou, Terrance Johnson, Hui Li, Nsoki Phambu, Alexander J. Ropelewski, Ouyang Lizhi |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Article Subject Polymers and Plastics biology 030106 microbiology technology industry and agriculture Bacillus cereus macromolecular substances Cellulase lcsh:Chemical technology biology.organism_classification Molecular biology Genome law.invention Gel permeation chromatography 03 medical and health sciences Cereus law Proteome biology.protein Recombinant DNA lcsh:TP1-1185 TOPO cloning |
Zdroj: | International Journal of Polymer Science, Vol 2017 (2017) |
ISSN: | 1687-9430 1687-9422 0000-0000 |
DOI: | 10.1155/2017/6192924 |
Popis: | In previous work, we reported on the isolation and genome sequence analysis ofBacillus cereusstrain tsu1 NCBI accession number JPYN00000000. The 36 scaffolds in the assembled tsu1 genome were all aligned withB. cereusB4264 genome with variations. Genes encoding for xylanase and cellulase and the cluster of genes in the poly-3-hydroxybutyrate (PHB) biosynthesis pathway were identified in tsu1 genome. The PHB accumulation inB. cereustsu1 was initially identified using Sudan Black staining and then confirmed using high-performance liquid chromatography. Physical properties of these PHB extracts, when analyzed with Raman spectra and Fourier transform infrared spectroscopy, were found to be comparable to the standard compound. The five PHB genes in tsu1(phaA,phaB,phaR,phaC,andphaP)were cloned and expressed with TOPO cloning, and the recombinant proteins were validated using peptide mapping of in-gel trypsin digestion followed by mass spectrometry analysis. The recombinantE. coliBL21 (DE3) (over)expressingphaCwas found to accumulate PHB particles. The cellulolytic activity of tsu1 was detected using carboxymethylcellulose (CMC) plate Congo red assay and the shift towards low-molecular size forms of CMC revealed by gel permeation chromatography in CMC liquid culture and the identification of a cellulase in the secreted proteome. |
Databáze: | OpenAIRE |
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