Literature DB >> 24435854

Draft Genome Sequence of the Bioelectricity-Generating and Dye-Decolorizing Bacterium Proteus hauseri Strain ZMd44.

Nan Wang1, I-Son Ng, Po Ting Chen, Yuzhe Li, Yi-Chung Chen, Bor-Yann Chen, Yinghua Lu.   

Abstract

Proteus hauseri ZMd44 (CGMCC 6746), as a crucial biodecolorizing, bioelectricity-generating, and copper-resistant bacterium, is distinguished from the urinary pathogens Proteus penneri and Proteus mirabilis. To further investigate the genetic functions of this strain, the genome sequence and annotation of its open reading frames, which consist of 3,875,927 bp (G+C content, 38.12%), are presented here.

Entities:  

Year:  2014        PMID: 24435854      PMCID: PMC3894268          DOI: 10.1128/genomeA.00992-13

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Proteus hauseri ZMd44 is a new classification of the Proteus genus (1), which was found in Lanyang Plain, northeast Taiwan. It has been used for application in microbe fuel cells (MFCs) with wastewater using azo dye Reactive Blue 160 (RBu160) (2). Moreover, the interactive characteristics of bioelectricity generation and dye decolorization in MFCs have been established (3). Recently, P. hauseri ZMd44 has been found to express McoA-laccase by induction with copper sulfate (4). Moreover, P. hauseri cells were significantly suppressed and swarming motility was inhibited with supplementation of Cu(II). This implies that its copper-related genes potentially contain vital therapeutic functions, since P. hauseri lost capabilities to cause swarming motility and urinary tract infections in the presence of Cu(II). This is why the genome sequencing for this new species is of great importance and significance. High-throughput DNA sequencing of P. hasueri ZMd44 was conducted on the Illumina GA IIx 90-bp paired-end platform, with an average insert size of 250 bp, at Yourgene Bioscience (Taiwan). In total, 14,455,522 reads were achieved, resulting in 3.73-fold genomic coverage. The reads were filtered to remove adapter sequences and achieve the quality trim of at least 35 bp. A draft genome was generated by de novo assembly, using a high-volume-read-accommodating algorithm by storing data in de Bruijn graphs (5). This genome is a single circular chromosome of 3,875,927 bp with a mean G+C content of 38.12%. Fifty-one contigs with an N50 value of 197,041 and a largest contig of 1,426,865 bp were constructed. Gene prediction using GeneMark (6) revealed a total of 3,147 open reading frames (ORFs). The predicted proteins were annotated by implementing a BLASTp search against the NCBI NR database. A comparative genome analysis of P. hauseri ZMd44 with the closely related Proteus mirabilis HI4320 (7) revealed that the strains are similar, with 2,274 known protein-coding genes, 490 hypothetical protein-coding genes, and 383 no-hits genes. The known coding genes for proteins and enzymes are involved in the three catalogues of biological process (44.9%), cellular component (23.5%), and molecular function (31.6%). On the other hand, only four ORFs encode proteins that are predicted to be involved in the copper resistance properties of P. hauseri ZMd44. The proteins are copper homeostasis protein CutC, copper resistance protein Crp, multicopper oxidase Mco, and repressor protein FtsI. Among these, the highest sequence identity of Crp to other pathogens microbes is only 33.3% with that of the PcoD from Escherichia coli strain K-12 substrain W3110 (accession no. YP_490102), followed by 12.8% with that of CopD from Shewanella putrefaciens CN-32 (accession no. YP_001181786). Thus, the lower similarity of the copper-resistant protein has suggested that Crp is the key protein of P. hauseri ZMd44 for copper resistance. This draft genome sequence helps accelerate the understanding of the characteristics of this strain not only in application of MFC and bioremediation processes, but also by potentially using the copper-related genes in therapeutic therapy of urinary tract infection caused by Proteus  species.

Nucleotide sequence accession number.

The whole-genome shotgun project for P. hauseri ZMd44 has been deposited in GenBank under the accession no. AWXP00000000.
  7 in total

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Authors:  J Besemer; M Borodovsky
Journal:  Nucleic Acids Res       Date:  1999-10-01       Impact factor: 16.971

2.  Velvet: algorithms for de novo short read assembly using de Bruijn graphs.

Authors:  Daniel R Zerbino; Ewan Birney
Journal:  Genome Res       Date:  2008-03-18       Impact factor: 9.043

3.  Understanding interactive characteristics of bioelectricity generation and reductive decolorization using Proteus hauseri.

Authors:  Bor-Yann Chen; Yu-Min Wang; I-Son Ng
Journal:  Bioresour Technol       Date:  2010-09-17       Impact factor: 9.642

4.  Assessment upon azo dye decolorization and bioelectricity generation by Proteus hauseri.

Authors:  Bor-Yann Chen; Meng-Meng Zhang; Chang-Tang Chang; Yongtao Ding; Kae-Long Lin; Chyow-San Chiou; Chung-Chuan Hsueh; Huizhong Xu
Journal:  Bioresour Technol       Date:  2010-02-13       Impact factor: 9.642

5.  Classification of Proteus vulgaris biogroup 3 with recognition of Proteus hauseri sp. nov., nom. rev. and unnamed Proteus genomospecies 4, 5 and 6.

Authors:  C M O'Hara; F W Brenner; A G Steigerwalt; B C Hill; B Holmes; P A Grimont; P M Hawkey; J L Penner; J M Miller; D J Brenner
Journal:  Int J Syst Evol Microbiol       Date:  2000-09       Impact factor: 2.747

6.  Copper ion-stimulated McoA-laccase production and enzyme characterization in Proteus hauseri ZMd44.

Authors:  Xuesong Zheng; I-Son Ng; Chiming Ye; Bor-Yann Chen; Yinghua Lu
Journal:  J Biosci Bioeng       Date:  2012-11-13       Impact factor: 2.894

7.  Complete genome sequence of uropathogenic Proteus mirabilis, a master of both adherence and motility.

Authors:  Melanie M Pearson; Mohammed Sebaihia; Carol Churcher; Michael A Quail; Aswin S Seshasayee; Nicholas M Luscombe; Zahra Abdellah; Claire Arrosmith; Becky Atkin; Tracey Chillingworth; Heidi Hauser; Kay Jagels; Sharon Moule; Karen Mungall; Halina Norbertczak; Ester Rabbinowitsch; Danielle Walker; Sally Whithead; Nicholas R Thomson; Philip N Rather; Julian Parkhill; Harry L T Mobley
Journal:  J Bacteriol       Date:  2008-03-28       Impact factor: 3.490

  7 in total

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