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. 2023 Jan 18;47:108919. doi: 10.1016/j.dib.2023.108919

Complete genome sequence data of Leuconostoc mesenteroides KNU-2 and Weissella hellenica MBEL1842 isolated from kimchi

JA Yoon a, SY Kwun a, EH Park b, MD Kim b,c,
PMCID: PMC9932316  PMID: 36819902

Abstract

Kimchi, a traditional Korean fermented food, contains many lactic acid bacteria. Leuconostoc mesenteroides KNU-2 strain with low-temperature tolerance and Weissella hellenica MBEL1842 with antibacterial activity were isolated from kimchi. The genomes of L. mesenteroides KNU-2 and W. hellenica MBEL1842 are composed of one circular chromosomal genome of 1,973,419 bp (37.9% G+C content) and 1,887,056 bp (37.9% G+C content), as well as four and one plasmids, respectively, The sequence data of the strains were deposited in GenBank under the accession numbers CP089782 (L. mesenteroides KNU-2) and CP086020 (W. hellenica MBEL1842).

Keywords: Complete genome, Kimchi, Lactic acid bacteria, Leuconostoc mesenteroides, Weissella hellenica


Specifications Table

Subject Genetics: General
Specific subject area Genomics and Molecular Biology
Type of data Table and Figure
How the data were acquired The PacBio RSII platform was used for genome sequencing. PacBio long-reads of L. mesenteroides KNU-2 were assembled using RS HGAP(v3.0) and annotated using Prokka (v1.12b), while those of W. hellenica MBEL1842 were assembled using FALCON (v.2.1.4) and annotated using Prokka (v1.12b).
Data format Raw and analyzed
Description of data collection Genomic DNA of L. mesenteroides KNU-2 and W. hellenica MBEL1842 was extracted and used.
Data source location • Institution: Kangwon National University
• City/Region: Chuncheon, Kangwon-do
• Country: Republic of Korea
• Latitude and longitude: 37°87′ N and 127°74′ E
Data accessibility The draft genome sequence of L. mesenteroides KNU-2 was deposited in GenBank under the following Biosample, Bioproject, Sequence Read Archive and GenBank accession number, SAMN10492388 (https://www.ncbi.nlm.nih.gov/biosample/?term=SAMN10492388), PRJNA507406 (https://www.ncbi.nlm.nih.gov/bioproject/PRJNA507406), SRX12232645 (https://www.ncbi.nlm.nih.gov/sra/SRX12232645),
and CP089782 (https://www.ncbi.nlm.nih.gov/nuccore/CP089782).
That of W. hellenica MBEL1842 was deposited under SAMN13968964 (https://www.ncbi.nlm.nih.gov/biosample/?term=SAMN13968964), PRJNA604418 (https://www.ncbi.nlm.nih.gov/bioproject/604418), SRX12745381-SRX12745386 (https://www.ncbi.nlm.nih.gov/sra/?term=SRP342772) and CP086020 (https://www.ncbi.nlm.nih.gov/nuccore/CP086020).

Value of the Data

  • The genome sequence of L. mesenteroides KNU-2 and W. hellenica MBEL1842 provides fundamental knowledge about genes related to lactic acid bacteria isolated from kimchi.

  • The genome data of the strains will be useful for comparative genomic analysis with other lactic acid bacteria.

  • The data can be useful in understanding the characterization of enzymes and genes related to kimchi fermentation.

1. Data Description

Kimchi is a traditional Korean fermented food consisting of vegetables such as Chinese cabbage, radish, and various ingredients [3]. Lactic acid bacteria (LAB), such as Leuconostoc, Lactobacillus, and Weissella genera, play an important role in kimchi fermentation [4,9]. Therefore, LAB are considered fermentation starters that produce standardized, high-quality kimchi [9]. L. mesenteroides KNU-2 strain with low-temperature tolerance and W. hellenica MBEL1842 with antibacterial activity were isolated from kimchi.

The PacBio reads of L. mesenteroides KNU-2 and W. hellenica MBEL1842 were assembled. Only the L. mesenteroides KNU-2 reads were assembled using RS HGAP (v3.0) to make a circular genome [1]. However, W. hellenica MBEL1842 reads were then assembled again using Falcon (v2.1.4) to obtain a circular genome [2]. The genome coverage of L. mesenteroides KNU-2 was 560 × and that of W. hellenica MBEL1842 was 366 ×.

Table 1 summarizes the genomic features of L. mesenteroides and W. hellenica strains. The genome of L. mesenteroides KNU-2 comprises one circular chromosomal genome of 1973,419 bp (37.9% G+C content) and four circular plasmids. The chromosome contains 1957 predicted protein-coding, 12 rRNA, and 71 tRNA genes. The genome of W. hellenica MBEL1842 was identified as a 1,887,056 bp (36.9% G+C content) circular chromosome with one circular plasmid. The chromosome has 1,779 predicted protein-coding, 25 rRNA, and 76 tRNA genes. The average nucleotide identity (ANI) value for L. mesenteroides KNU-2 and other L. mesenteroides strains was over 99%, indicating a high species boundary value (ANI > 95%) (Fig. 2) [8]. The W. hellenica MBEL1842 and other W. hellenica strains also showed a high ANI value of over 99% (Fig. 3). The whole-genome comparisons of L. mesenteroides (Fig. 4) and W. hellenica strains (Fig. 5) showed high synteny and no large rearrangements.

Table 1.

Genomic features of L. mesenteroides and W. hellenica strains.

Lactic acid bacteria Strain Length (bp) G+C content (%) Protein-coding genes rRNA genes tRNA genes Plasmid No. GenBank No. Refs.
L. mesenteroides KNU-2 1,973,419 37.9 1,957 12 71 4 CP089782 This study
LK151 2,090,103 37.8 1,974 9 67 3 AP017936 [6]
ATCC8293 2,038,396 37.7 1,925 12 70 1 CP000414 [10]
J18 1,900,740 37.8 1,769 12 70 4 CP003101 [5]
DRC1506 1,893,478 37.7 1,707 12 70 3 CP014611 [7]

W. hellenica MBEL1842 1,887,056 36.9 1,779 25 76 1 CP086020 This study
0916–4–2 1,875,603 38.9 1,834 25 76 2 CP033608 [12]
CBA3632 1,900,683 36.8 1,834 25 75 4 CP042399 -

Fig. 2.

Fig 2

Heatmap generated with Ortho-ANI values between Leuconostoc mesenteroides KNU-2 and other closely related species.

Fig. 3.

Fig 3

The Heatmap of the Ortho-ANI values of W. hellenica MBEL1842 and related Weissella species.

Fig. 4.

Fig 4

Whole-genome alignment of Leuconostoc mesenteroides strains.

Fig. 5.

Fig 5

Whole-genome alignment of Weissella hellenica strains.

The genome sequence of L. mesenteroides KNU-2 was deposited in GenBank under the accession number CP089782 (https://www.ncbi.nlm.nih.gov/nuccore/CP089782) and W. hellenica MBEL1842 was deposited under the accession number CP086020 (https://www.ncbi.nlm.nih.gov/nuccore/CP086020). The genome sequence data provide essential information for understanding LAB in kimchi.

2. Experimental Design, Materials, and Methods

The L. mesenteroides KNU-2 (KCTC18324P) and W. hellenica MBEL1842 strains were cultured in MRS (de Man, Rogosa and Sharpe) broth at 37 °C for 24 h. Genomic DNA was extracted from the strains grown to an exponential phase using the G-DEX™IIc Genomic DNA Extraction kit (iNtRON, Daejeon, Korea). Whole-genome sequencing was performed using the PacBio RSII platform (Pacific Biosciences, CA, USA). If it was estimated that the total number of bases in the PacBio reads would result in less than 100 × genome coverage, additional sequencing was performed, and all the output raw data were used for assembly.

The reads of L. mesenteroides KNU-2 and W. hellenica MBEL1842 were assembled using RS HGAP (v3.0) and FALCON (v2.1.4), respectively, [1,2]. Polishing was performed using the Quiver algorithm of SMRT® analysis (v2.3.0) and the assessment was performed using BUSCO (v3.0) [11]. Gene prediction was performed using Prokka (v1.12b) to predict and annotate the open reading frame [13]. Fig. 1 shows the whole-genome sequencing steps and the parameters.

Fig. 1.

Fig 1

Steps and parameters of whole-genome sequencing.

The ANI values for closely related species were calculated using the Orthologous Average Nucleotide Identity Software Tool (OAT). Whole-genome alignment of strains was visualized using the CLC Genomics Workbench 20.0.4 (CLC bio) software program.

Ethics Statements

Not applicable.

CRediT authorship contribution statement

J.A. Yoon: Methodology, Software, Data curation, Writing – original draft, Visualization. S.Y. Kwun: Methodology, Software, Data curation, Writing – original draft. E.H. Park: Writing – review & editing, Data curation. M.D. Kim: Conceptualization, Supervision, Funding acquisition.

Declaration of Competing Interest

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgments

This work was supported by the “Cooperative Research Program for Agriculture Science & Technology Development (Project No. PJ009477)”, Rural Development Administration Republic of Korea, and the Ministry of Trade Industry, and Energy (MOTIE), Korea, under the “Regional Specialized Industry Development Program” (reference number P0002815) supervised by the Korea Institute for Advancement of Technology (KIAT).

Data Availability

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Data Availability Statement


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