DOI QR코드

DOI QR Code

Complete genome sequences of Lactococcus lactis JNU 534, a potential food and feed preservative

  • Sangdon, Ryu (Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Science, Seoul National University) ;
  • Kiyeop, Kim (Division of Animal Science, Chonnam National University) ;
  • Dae-Yeon, Cho (Elim Land Co., Ltd) ;
  • Younghoon, Kim (Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Science, Seoul National University) ;
  • Sejong, Oh (Division of Animal Science, Chonnam National University)
  • Received : 2022.04.26
  • Accepted : 2022.05.06
  • Published : 2022.05.31

Abstract

A new bacteriocin-producing lactic acid bacteria isolated from kimchi was identified as Lactococcus lactis JNU 534, presenting preservative properties for foods of animal origin. In this study, we present the complete genome sequence of the bacterial strain JNU 534. The final complete genome assembly consists of one circular chromosome (2,443,687 bp [base pair]) with an overall GC (guanine-cytosine) content of 35.2%, one circular plasmid sequence (46,387bp) with a GC content of 34.5%, and one circular contig sequence (7,666 bp) with a GC content of 36.2%.

Keywords

Lactococcus lactis is a homo-fermentative, Gram-positive cocci and is traditionally used around the world in the fermentation process of dairy products, kimchi and silage [1]. Recent research show that L. lactis suppressed methane production in ruminant because these bacteria had the ability to inhibit rumen methanogens [2].

Among the antibacterial compounds produced by lactic acid bacteria, bacteriocin is a natural proteinaceous substance that inhibits the growth of pathogenic bacteria present in food and whose production can be controlled through genetic manipulation [3]. When ingested, it is decomposed by proteolytic enzymes in the digestive system and is harmless to the human body. Therefore, bacteriocin is attracting attention as a natural, non-toxic preservative produced by microorganisms with potential applications in the food industry [4]. Many bacteriocins have been identified and a few under the same Lactobacillus genus are known to produce different types with different activity ranges [5]. Nisin, a representative bacteriocin produced by Lactococcus lactis subsp. lactis, is a polypeptide composed of 34 amino acids that is non-toxic to humans. Owing to its characteristics, its application as a food preservative has been expanded, and it is currently permitted as a food additive in several countries [6].

In the present study, L. lactis JNU 534 producing bacteriocin (previously identified as Pediococcus damnosus) was isolated from kimchi [7]. This strain was cultured in de Man, Rogosa, and Sharpe (MRS) broth (Difco, Sparks, MD, USA) at 37℃ for 24 h. Total genomic DNA of L. lactis JNU 534 was extracted using the PureHelixTM Genomic DNA prep kit (Nanohelix, Daejeon, Korea) according to the instructions of the manufacturer. The concentration of extracted DNA and quality were measured using the Qubit 2.0 Fluorometer (Invitrogen, Carlsbad, CA, USA) and the SpectraMax ABS Plus microplate reader (Molecular devices, San Jose, CA, USA), respectively.

The complete genome of L. lactis JNU 534 was sequenced using the PacBio Sequel system (Pacific Biosciences, Menlo Park, CA, USA) and the Illumina HiSeq (151 × 2 base pair [bp] paired-end sequencing) platforms at Macrogen (Macrogen, Seoul, Korea). The preparation of sequencing libraries for PacBio sequencing was performed using the SMRTbellTM template prep kit 1.0 (Pacific Biosciences) and Illumina sequencing was performed using the NEBNext® UltraTM DNA library prep kit for Illumina® (NEB, Ipswich, MA,USA), according to the instructions of the manufacturers. A total number of 131,035 reads with a mean subread length of 9,196 bases (N50, 10,823 bases) were obtained with PacBio sequencing, and 33,461,064 paired-end reads totaling 5,052,620,664 bp were obtained with Illumina sequencing. De novo assembly was carried out using microbial assembly application within the PacBio SMRT analysis pipeline 8.0 with default options (http://www.pacb.com/devnet/). The Microbial Assembly Application can determine whether contigs are circular and automatically rotate each contig start site as the origin of replication. Assembly error correction was performed using Pilon version 1.21 [8]. The completeness of the genome assembly was assessed using the Benchmarking Universal Single-Copy Orthologous suite (BUSCO, v5.1.3) [9]. The chromosome, plasmid, and contig annotation were performed using rapid prokaryotic genome annotation (Prokka, v1.13) [10].

The complete genome sequence of L. lactis JNU 534 consists of one circular chromosome (2,443,687 bp) with an overall GC (guanine-cytosine) content of 35.2%, one circular plasmid sequence (46,387bp) with a GC content of 34.5%, and one contig sequence (7,666 bp) with a GC content of 36.2% (Table 1). A total of 2511 predicted genes, including 19 rRNA and 62 tRNA, were identified on the genome, of which 2455, 49, and 7 coding DNA sequences were located on the chromosome, plasmid, and contig, respectively. (Fig. 1) The genomic information of L. lactis JNU 534 may guide future research on the characteristics and stability of this strain and confirm its applicability as a preservative of foods of animal origin.

Table 1. Genome features of Lactococcus lactis JNU 534

DMJGDA_2022_v64n3_599_t0001.png 이미지

bp, base pair; G, guanine; C, cytosine; CDSs, coding DNA sequences; tRNA, transfer RNA; rRNA, ribosomal RNA.

DMJGDA_2022_v64n3_599_f0001.png 이미지

Fig. 1. Circular chromosome, plasmid, and contig maps of Lactococcus lactis JNU 534. Marked characteristics are shown as (from the periphery to the center): coding DNA sequences on forward strand, coding DNA sequences on reverse strand, tRNA, rRNA, GC content, and GC skew. (A) Chromosome, (B) Plasmid, (C) Contig. bp, base pair; tRNA, transfer RNA; rRNA, ribosomal RNA; G, guanine; C, cytosine.

NUCLEOTIDE SEQUENCE ACCESSION NUMBER

The complete chromosome, plasmid, and contig sequences of L. lactis JNU 534 have been deposited in GenBank under the accession numbers CP095737.1, CP095738.1, and CP095739.1, respectively. The BioProject and BioSample accession numbers are PRJNA826729 and SAMN27578898.

References

  1. van Hylckama Vlieg JET, Rademaker JLW, Bachmann H, Molenaar D, Kelly WJ, Siezen RJ. Natural diversity and adaptive responses of Lactococcus lactis. Curr Opin Biotechnol. 2006;17:183-90. https://doi.org/10.1016/j.copbio.2006.02.007
  2. Huyen NT, Martinez I, Pellikaan W. Using lactic acid bacteria as silage inoculants or directfed microbials to improve in vitro degradability and reduce methane emissions in dairy cows. Agronomy. 2020;10:1482. https://doi.org/10.3390/agronomy10101482
  3. Nes IF, Johnsborg O. Exploration of antimicrobial potential in LAB by genomics. Curr Opin Biotechnol. 2004;15:100-4. https://doi.org/10.1016/j.copbio.2004.02.001
  4. Jack RW, Tagg JR, Ray B. Bacteriocins of gram-positive bacteria. Microbiol Rev. 1995;59:171-200. https://doi.org/10.1128/mr.59.2.171-200.1995
  5. Oh S, Roh H, Ko HJ, Kim S, Kim KH, Lee SE, et al. Complete genome sequencing of Lactobacillus acidophilus 30SC, isolated from swine intestine. Am Soc Microbiol. 2011;193:2882-3. https://doi.org/10.1128/JB.00343-11
  6. Kim WJ. Bacteriocins of lactic acid bacteria: their potentials as food biopreservative. Food Rev Int. 1993;9:299-313. https://doi.org/10.1080/87559129309540961
  7. Lee JW, Han SM, Yun BH, Oh SJ. Characteristics and partial purification of a bacteriocin produced by Pediococcus damnosus JNU 534. Food Sci Anim Resour. 2011;31:952-9. https://doi.org/10.5851/kosfa.2011.31.6.952
  8. Walker BJ, Abeel T, Shea T, Priest M, Abouelliel A, Sakthikumar S, et al. Pilon: an integrated tool for comprehensive microbial variant detection and genome assembly improvement. PLOS ONE. 2014;9:e112963. https://doi.org/10.1371/journal.pone.0112963
  9. Simao FA, Waterhouse RM, Ioannidis P, Kriventseva EV, Zdobnov EM. BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics. 2015;31:3210-2. https://doi.org/10.1093/bioinformatics/btv351
  10. Seemann T. Prokka: rapid prokaryotic genome annotation. Bioinformatics. 2014;30:2068-9. https://doi.org/10.1093/bioinformatics/btu153