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. 2020 Apr 16;9(16):e00158-20. doi: 10.1128/MRA.00158-20

Draft Genome Sequences of Three Amino Acid-Secreting Lactococcus lactis Strains

Jhonatan A Hernandez-Valdes a, Anne de Jong a, Jan Kok a, Oscar P Kuipers a,
Editor: David A Baltrusb
PMCID: PMC7163014  PMID: 32299876

Three Lactococcus lactis strains with the ability to secrete various amino acids (leucine, isoleucine, methionine, valine, glutamic acid, and histidine) were sequenced in order to identify the mechanisms involved in the secretion. Amino acids contribute to flavor formation; therefore, bacterial strains with this ability are relevant for the food industry.

ABSTRACT

Three Lactococcus lactis strains with the ability to secrete various amino acids (leucine, isoleucine, methionine, valine, glutamic acid, and histidine) were sequenced in order to identify the mechanisms involved in the secretion. Amino acids contribute to flavor formation; therefore, bacterial strains with this ability are relevant for the food industry.

ANNOUNCEMENT

Bacteria secrete several compounds during growth, as well as in stationary phase. Some of these compounds are relevant for the food industry, for instance in the large-scale production of amino acids that find application as feed additives, flavor-promoting compounds, or ingredients in pharmaceuticals (1 3). Moreover, the relationship between amino acids and flavor formation has been studied extensively in lactic acid bacteria used in dairy fermentations, in order to understand and to improve the organoleptic properties of dairy products (4, 5). In particular, Lactococcus lactis is widely used as a starter culture for the manufacture of buttermilk, quark, and a wide variety of cheeses (6). Its proteolytic system provides the cells with essential amino acids from casein (7). The amino acids, obtained from casein degradation, are either flavor compounds or flavor precursors (8, 9).

In this work, we report three amino acid-secreting L. lactis strains from the laboratory collection of the molecular genetics department at the University of Groningen (Groningen, The Netherlands) (J. A. Hernandez-Valdes, manuscript in preparation). The strains were originally isolated from dairy environments. The L. lactis C17 strain was obtained from the NIZO collection, the L. lactis NCDO176 strain was obtained from the DSMZ collection, and the L. lactis WW4 strain was obtained from the MolGen collection. A single colony of each strain growing on an LM17 agar plate was selected, grown as a standing culture in 5 ml of M17 broth supplemented with 0.5% (wt/vol) lactose (LM17 broth), and incubated overnight at 30°C. Cells from the three cultures were collected by centrifugation at 10,000 rpm for 3 min in a Microfuge 16 centrifuge (Beckman Coulter, Woerden, The Netherlands). Genomic DNA was isolated with a GenElute bacterial genome DNA kit (Sigma-Aldrich, Munich, Germany) according to the manufacturer’s instructions.

The genomes of the lactococcal strains were paired-end sequenced at the Beijing Genomics Institute (Copenhagen, Denmark) on a BGISEQ-500 platform. A total of 5 million paired-end reads (150 bp) were generated. FastQC version 0.11.5 (10) was used to examine the quality of the reads, and low-quality reads were removed with Trimmomatic version 0.38 (11). Subsequently, SPAdes version 3.11.1 (12) was used with default parameters to perform a de novo paired-end assembly for each genome, resulting in the draft genome sequences. The coverages of the three sequenced genomes all exceeded 150×. The characteristics of the assemblies and genome features obtained are described in Table 1. Taxonomic assignment of reads was performed with Kraken version 2.0.7 (13). The Rapid Annotations using Subsystems Technology (RAST) server (14) and Prokka (15) were used to annotate the genomes. Further analysis of the genomes, in order to discover the mechanisms underlying amino acid secretion by these bacteria, is under way.

TABLE 1.

Genome features and accession numbers for the three Lactococcus lactis strains

Lactococcus lactis subsp. lactis strain Genome size (bp) G+C content (%) No. of coding sequences No. of contigs GenBank accession no. SRA accession no.
C17 2,552,877 35.0 2,717 130 WJUK00000000 SRR10203129
NCDO176 2,445,329 35.1 2,579 120 WJUL00000000 SRR10203130
WW4 2,553,867 34.9 2,716 132 WJUM00000000 SRR10203131

Data availability.

The genome sequences of the three Lactococcus lactis strains have been deposited in GenBank under the accession numbers listed in Table 1. The raw reads were submitted to the Sequence Read Archive (SRA) under the accession numbers listed in Table 1.

ACKNOWLEDGMENT

J.A.H.-V. and O.P.K. were supported by the Netherlands Organization for Scientific Research (research program TTW, grant 13858).

REFERENCES

  • 1.Krämer R. 1994. Secretion of amino acids by bacteria: physiology and mechanism. FEMS Microbiol Rev 13:75–93. doi: 10.1016/0168-6445(94)90102-3. [DOI] [Google Scholar]
  • 2.Hirasawa T, Shimizu H. 2016. Recent advances in amino acid production by microbial cells. Curr Opin Biotechnol 42:133–146. doi: 10.1016/j.copbio.2016.04.017. [DOI] [PubMed] [Google Scholar]
  • 3.Ma Q, Zhang Q, Xu Q, Zhang C, Li Y, Fan X, Xie X, Chen N. 2017. Systems metabolic engineering strategies for the production of amino acids. Synth Syst Biotechnol 2:87–96. doi: 10.1016/j.synbio.2017.07.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Juillard V, Le Bars D, Kunji ERS, Konings WN, Gripon JC, Richard J. 1995. Oligopeptides are the main source of nitrogen for Lactococcus lactis during growth in milk. Appl Environ Microbiol 61:3024–3030. doi: 10.1128/AEM.61.8.3024-3030.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Niven GW, Knight DJ, Mulholland F. 1998. Changes in the concentrations of free amino acids in milk during growth of Lactococcus lactis indicate biphasic nitrogen metabolism. J Dairy Res 65:101–107. doi: 10.1017/S002202999700263X. [DOI] [PubMed] [Google Scholar]
  • 6.Laroute V, Tormo H, Couderc C, Mercier-Bonin M, Le Bourgeois P, Cocaign-Bousquet M, Daveran-Mingot M-L. 2017. From genome to phenotype: an integrative approach to evaluate the biodiversity of Lactococcus lactis. Microorganisms 5:27. doi: 10.3390/microorganisms5020027. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Savijoki K, Ingmer H, Varmanen P. 2006. Proteolytic systems of lactic acid bacteria. Appl Microbiol Biotechnol 71:394–406. doi: 10.1007/s00253-006-0427-1. [DOI] [PubMed] [Google Scholar]
  • 8.Ayad EHE, Verheul A, De Jong C, Wouters JTM, Smit G. 1999. Flavour forming abilities and amino acid requirements of Lactococcus lactis strains isolated from artisanal and non-dairy origin. Int Dairy J 9:725–735. doi: 10.1016/S0958-6946(99)00140-5. [DOI] [Google Scholar]
  • 9.Smit G, Smit BA, Engels W. 2005. Flavour formation by lactic acid bacteria and biochemical flavour profiling of cheese products. FEMS Microbiol Rev 29:591–610. doi: 10.1016/j.fmrre.2005.04.002. [DOI] [PubMed] [Google Scholar]
  • 10.Andrews S. 2010. FastQC: a quality control tool for high throughput sequence data. http://www.bioinformatics.babraham.ac.uk/projects/fastqc.
  • 11.Bolger AM, Lohse M, Usadel B. 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30:2114–2120. doi: 10.1093/bioinformatics/btu170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Nurk S, Bankevich A, Antipov D, Gurevich A, Korobeynikov A, Lapidus A, Prjibelsky A, Pyshkin A, Sirotkin A, Sirotkin Y, Stepanauskas R, McLean J, Lasken R, Clingenpeel SR, Woyke T, Tesler G, Alekseyev MA, Pevzner PA. 2013. Assembling genomes and mini-metagenomes from highly chimeric reads, p 158–170. In Deng M, Jiang R, Sun F, Zhang X (ed), Research in computational molecular biology, RECOMB 2013: lecture notes in computer science, vol 7821 Springer, Berlin, Germany. [Google Scholar]
  • 13.Wood DE, Salzberg SL. 2014. Kraken: ultrafast metagenomic sequence classification using exact alignments. Genome Biol 15:R46. doi: 10.1186/gb-2014-15-3-r46. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Aziz RK, Bartels D, Best A, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: Rapid Annotations using Subsystems Technology. BMC Genomics 9:75. doi: 10.1186/1471-2164-9-75. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Seemann T. 2014. Prokka: rapid prokaryotic genome annotation. Bioinformatics 30:2068–2069. doi: 10.1093/bioinformatics/btu153. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The genome sequences of the three Lactococcus lactis strains have been deposited in GenBank under the accession numbers listed in Table 1. The raw reads were submitted to the Sequence Read Archive (SRA) under the accession numbers listed in Table 1.


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