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Genome analysis of Brevundimonas diminuta DB-19
HONG Yuehui, FAN Hongdi, WU Jiayan, XIONG Qunying, WANG Jianghai
2025, 42 (4):
101.
doi: 10.3969/j.issn.2095-1736.2025.04.101
To reveal the genetic background and the mechanisms of petroleum hydrocarbon degradation inBrevundimonas diminutaDB-19, Illumina sequencing, Nanopore sequencing and bioinformatics
methods were used to analyze the genome of strain DB-19. The complete
genome sequences of strain DB-19 were obtained. One contig was obtained
after genome assembly, and its type was circular chromosome. The genome
size was 3589837 bp, and the GC content was 67.38%. A total of 3609
genes coding for proteins were predicted. Fifty-two tRNA genes were
found using the tRNAscan-SE. The number of genes coding for 16S rRNA, 5S
rRNA, 23S rRNA and sRNA was 2, 2, 2 and 1, respectively. Gene function
annotation showed that the number of genes annotated in the NR,
Swiss-Prot, COG, GO, Pfam, PHI, VFDB, ARDB, KEGG and CAZy databases was
3401, 2189, 2854, 1714, 2817, 812, 629, 1, 3193 and 89, respectively.
According to the identified genes, it was inferred that terminal
oxidative pathway was the main pathway for the degradation of n-alkanes
in strain DB-19, and that homogentisate pathway and β-ketoadipate
pathway played main roles in the degradation of aromatic compounds.
These results deepened our understanding ofB. diminuta,
contributed to designing more effective methods for the remediation of
petroleum pollution, and provided important reference for studying the
mechanisms of pollutant degradation in other microorganisms.
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