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Microbiology and Biotechnology Letters

Genome Report(Note)

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Genome Report  |  Genome Report

Microbiol. Biotechnol. Lett. 2024; 52(1): 94-96

https://doi.org/10.48022/mbl.2312.12001

Received: December 4, 2023; Revised: January 10, 2024; Accepted: January 19, 2024

Complete Genome Sequence of Pseudarthrobacter sp. IC2-21, a Fluquinconazole-Degrading Soil Bacterium

Myoungjoo Riu, Songhwa Kim, and Jaekyeong Song*

Agricultural Microbiology Division, National Institute of Agricultural Sciences (NAS), Rural Development Administration (RDA), Wanju 55365, Republic of Korea

Correspondence to :
Jaekyeong Song        mgjksong@korea.kr

Pseudarthrobacter sp. IC2-21 is isolated from the greenhouse soil in Icheon, Gyeonggi, Korea. This strain IC2-21 is a first fluquinconazole degrading soil bacterium. We analyze the whole genome sequence of Pseudarthrobacter sp. IC2-21. The sequence analysis revealed that Pseudarthrobacter sp. IC2-21 possesses a single 4,265,009 bps circular chromosome with a DNA G+C-content of 65.4%. This chromosome contains 3,942 protein-coding sequences and 12 rRNA and 51 tRNA genes. In the result of sequence analysis, it is revealed that strain IC2-21 possessed genes coding the triazole pesticides degradation related enzymes, such as oxygenase, and fluquinconazole degradation related genes.

Keywords: Pseudarthrobacter sp. IC2-21, genome, fluquinconazole, degradation

Triazole fungicides are effective against a diverse range of fungal pathogens in crops and have been increasingly used in agricultural practices for high yields and product quality [1]. Fluquinconazole is effective at controlling fungal diseases that cause serious damage to crops, such as the take-all disease and Septoria tritici blotch in wheat [2, 3]. However, triazole pesticides can cause problems if they persist in the environment [4]. Triazole pesticides are toxic to soil microorganisms. This can significantly alter the structure of soil microbial communities and decrease soil enzyme activity [5]. These changes can affect the soil health and fertility [4]. Therefore, the use of triazole pesticides should be carefully monitored. As part of the efforts to manage pesticide residues in the soil, recent research has been conducted on microorganisms that decompose pesticides [6].

The strain IC2-21 of Pseudarthrobacter sp. was isolated from soil in a greenhouse and cultivated in tryptic soy broth at a temperature of 20℃ for a duration of 48 h. The conditions maintained were aerobic with a pH range between 6.0 and 10.0, with the optimal pH being 8.0. The genomic DNA was then extracted from the cultured cells of strain IC2-21 using a QIAamp DNA mini kit (Qiagen, Germany), following the guidelines provided by the manufacturer. The complete genome of the IC2-21 strain was sequenced utilizing the PacBio Sequel sequencing platform (Pacific Biosciences, USA) and the NovaSeq6000 platform (Illumina, USA) at Macrogen (Republic of Korea). The genome assembly was carried out using the Microbial Assembly Application provided (Macrogen), and the annotation was performed using the Prokaryotic Genome Annotation Pipeline from National Center for Biotechnology Information (NCBI) [7]. The complete genome sequence of strain IC2-21 was found to comprise 4,265,009 bps, with an average GC content of 65.4%. No plasmids were detected. The strain IC2-21 chromosome contained 3,942 protein-coding sequences, 12 rRNA genes and 51 tRNA genes (Table 1). The OrthoANI values, calculated using the OrthoANI algorithm version v0.93.1 [8], between the genome sequences of the P. sulfonivorans type strain and the IC2-21 were found to be 87.33% (Fig. 1). The genome of strain IC2-21 contained genes (pcaG and clcA) associated with the synthesis of protocatechuate 3,4-dioxygenase, which catalyzes the ring cleavage step in the breakdown of aromatic compounds [9], and genes related to the 3-oxoadipate CoA-transferase subunit (pcaI and pcaJ), catechol-2,3-dioxygenase (catE), and the 1,2-phenylacetyl-CoA epoxidase subunit (paaA). Additionally, the genome of strain IC2-21 contained genes similar to those encoding flavoprotein reductase. These included rutF, which encodes FMN reductase (a flavin reductase domain protein that binds to FMN); namA, which encodes NADPH dehydrogenase (also known as NADH flavin oxidoreductase); and fprA, which encodes NADPHferredoxin reductase. Flavoprotein reductase catalyzes the addition of two molecular oxygen atoms to the adjacent carbons of the aromatic ring, facilitating ring activation and subsequent oxidation [10], thereby potentially contributing to ring opening.

Table 1 . Genome features of Pseudarthrobacter sp. strain IC2-21.

Genome featuresChromosome
Genome size (bp)4,265,009
G + C content (%)65.4
Protein-coding genes (CDSs)3,942
Number of rRNAs12
Number of tRNAs51
ncRNAs3
Number of pseudogenes28
Plasmids0
Accession number (Genbank)CP139145

Figure 1.Genetic similarity test of Pseudarthrobacter sp. IC2-21. Unweighted Pair Group Method with Arithmeti Mean (UPGMA) tree and heatmap generated with OrthoANI values calculated from Orthologous Average Identity Tool (OAT) software. The scale bar indicates 2% sequence divergence.

Overall, sequencing analysis of the IC2-21 genome revealed that it possessed several genes involved in ring cleavage during the degradation of aromatic compounds. Therefore, this strain shows in the potential for use in bioremediation of fluquinconazole-contaminated soils.

트리아졸계 살균제인 플루퀸코나졸을 분해할 수 있는 Pseudarthrobacter sp. IC2-21 균주는 이천 지역의 비닐하우스 토양으로부터 분리하였다. IC2-21 균주의 전체 염기서열을 분석한 결과, 4,265,009 bps를 가진 단일 환형 염색체로서 G+C 함량은 65.4%로 구성되었다. 이 유전체는 3,884개의 단백질을 암호하는 염기서열을 가졌으며, 12개의 rRNA와 51개의 tRNA 유전자를 포함한다. 염기서열 분석 결과, IC2-21 균주는 플루퀸코나졸의 분해에 관여하는 효소인 oxygenase를 암호화하는 유전자를 가졌음을 밝혔다.

The whole genome sequence of strain IC2-21 described in this study has been deposited in the NCBI database under accession number CP139145. The strain was deposited to the Korean Agricultural Culture Collection under accession number KACC 81278BP.

This study was carried out with the financial support for the project titled “Research Program for Agricultural Science & Technology Development (Project No. RS-2020-RD008788)” provided by the National Institute of Agricultural Sciences, Rural Development Administration, Republic of Korea.

The authors have no financial conflicts of interest to declare.

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