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International Journal of Genomics
Volume 2017 (2017), Article ID 9481756, 12 pages
https://doi.org/10.1155/2017/9481756
Research Article

Exploration of Nitrate Reductase Metabolic Pathway in Corynebacterium pseudotuberculosis

1Institute of Biologic Sciences, Federal University of Minas Gerais, 31270-901 Belo Horizonte, MG, Brazil
2Center for Nuclear Energy in Agriculture, University of Sao Paulo, 13400-970 Piracicaba, SP, Brazil
3Escola de Veterinária, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil
4Departamento de Medicina Veterinária, Universidade Federal de Lavras, Lavras, MG, Brazil
5Centre for Genomics and Applied Gene Technology, Institute of Integrative Omics and Applied Biotechnology (IIOAB), Nonakuri, Purba Medinipur, West Bengal, India

Correspondence should be addressed to Sintia Almeida; moc.liamg@adiemlaaitnis, Andrey P. Lage; moc.liamg@11egalpa, and Vasco Azevedo; moc.liamg@notsiraocsav

Received 7 July 2016; Revised 2 October 2016; Accepted 23 October 2016; Published 20 February 2017

Academic Editor: Wen-Chi Chou

Copyright © 2017 Sintia Almeida et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Supplementary Material

Supplementary Figures 1 to 3 and Figure 7: Transmembrane helices prediction to NarI, NarK, NarT and NirK proteins, respectively, from C. pseudotuberculosis biovar Equi. Supplementary Figure 4: Transcription unit for the nrfHA genes into C. pseudotuberculosis biovar Equi. Supplementary Figure 5: Multiple sequence alignment of C. pseudotuberculosis biovar Equi nirK gene. Supplementary Figure 6: Amino acid sequence alignment of bacterial NirKs. Supplementary Figure 8: Comparative nitrogen metabolism between E.coli and C. pseudotuberculosis biovar Equi. In red pathway to E. coli, in green to C. pseudotuberculosis.  Supplementary Table 1:  Similarity sequence analysis of nirK gene of C. pseudotuberculosis and bacterial CuNiRs

  1. Supplementary Material