Literature DB >> 24831147

Complete Genome Sequence of Dyella jiangningensis Strain SBZ3-12, Isolated from the Surfaces of Weathered Rock.

Yuanyuan Bao1, Amy Ho Yan Kwok2, Linyan He3, Jingwei Jiang2, Zhi Huang1, Frederick Chi-Ching Leung2, Xiafang Sheng1.   

Abstract

Dyella jiangningensis strain SBZ3-12 can weather biotite and release Al and Fe from biotite under nutrient-poor conditions. Here, we report the first complete genome sequence of D. jiangningensis strain SBZ3-12, which may facilitate a better understanding of the molecular mechanism behind mineral weathering.
Copyright © 2014 Bao et al.

Entities:  

Year:  2014        PMID: 24831147      PMCID: PMC4022811          DOI: 10.1128/genomeA.00416-14

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Strain SBZ3-12 was isolated from surfaces of weathered mineral rocks using the dilution plating method. Based on our previous phenotypic, chemotaxonomic, and phylogenetic analysis, it is proposed that strain SBZ3-12 represents a novel species of the genus Dyella, which is designated Dyella jiangningensis sp. nov. (1). Mineral weathering experiments showed that strain SBZ3-12 was able to weather biotite and released more Al and Fe than the control. Despite decades of dedicated efforts by many scholars, controversies remain regarding the roles of microorganisms in mineral precipitation and weathering and the molecular mechanism behind the bio-degradation (2, 3). Here we present the whole-genome sequence of D. jiangningensis strain SBZ3-12. Genomic DNA of D. jiangningensis strain SBZ3-12 was isolated following the methods listed in Wilson’s study (4). The quality of DNA was examined using a NanoDrop2000 spectrophotometer (Thermo Scientific). The SBZ3-12 genome was sequenced using a 454 GS Junior pyrosequencing system (Roche) with ~25-fold coverage. One shotgun-genome run and one 8-kb library span paired-end run were conducted, yielding 373,571 reads. These reads were assembled into 39 large contigs (length, >500 bp) using the Newbler 2.4 assembly software program (Roche). Gaps between large contigs were filled by Sanger sequencing of the PCR products by means of an ABI 3730XL capillary sequencer and subsequent assembly using SeqMan software (DNASTAR). The open reading frames (ORFs) and rRNA and tRNA genes were annotated by the NCBI Prokaryotic Genome Automatic Annotation Pipeline (PGAAP) (5). Functional classification was performed by aligning predicted proteins to the Clusters of Orthologous Groups (COG) database (6). All predicted genes were compared to a nonredundant (nr) protein database in NCBI using BLASTX (7), with E values of 1 × 10−5 and filtering at 20% match identity and 90% alignment length. Metabolic pathways were analyzed by a bi-directional best-hit method on the KEGG web server (8). D. jiangningensis strain SBZ3-12 has one chromosome, which is 5,396,991 bp in size with a G+C content of 64.22%. The chromosome has 4,666 predicted coding sequences (CDS), and 59 RNAs were identified, including 52 tRNAs, 6 rRNAs, and 1 non-coding RNA (ncRNA). As for the chromosome genes, 61.23% were assigned to specific COGs, and approximately 74.07% of the genes were assigned to a KEGG orthologous number and were involved in 202 predicted metabolic pathways. Moreover, 36 CDS encoding outer membrane receptor proteins (involved mostly in Fe transport) were annotated and may play important roles in mineral weathering (9).

Nucleotide sequence accession number.

The complete genome sequence of D. jiangningensis strain SBZ3-12 has been deposited at DDBJ/EMBL/GenBank database under the accession no. CP007444. The version described in this paper is the first version.
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