Cited by 59Genomics and Phylogenetic StudiesAlgal biology and biofuel productionPhotosynthetic Processes and Mechanisms

Draft genome sequence of Arthrospira platensis C1 (PCC9438)

Open access
Cheevadhanarak, Supapon, Paithoonrangsarid, Kalyanee, Prommeenate, Peerada, Kaewngam, Warunee, Musigkain, Apiluck, Tragoonrung, Somvong, Tabata, Satoshi, Kaneko, Takakazu +20 more·2012·Standards in Genomic Sciences

Abstract

Arthrospira platensis is a cyanobacterium that is extensively cultivated outdoors on a large commercial scale for consumption as a food for humans and animals. It can be grown in monoculture under highly alkaline conditions, making it attractive for industrial production. Here we describe the complete genome sequence of A. platensis C1 strain and its annotation. The A. platensis C1 genome contains 6,089,210 bp including 6,108 protein-coding genes and 45 RNA genes, and no plasmids. The genome information has been used for further comparative analysis, particularly of metabolic pathways, photosynthetic efficiency and barriers to gene transfer.

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Crossref · 10.4056/sigs.2525955

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  • A draft genome of a cold-resistant spirulina strain obtained from Solenoye Lake in Siberia did not identify any unique genes related to its tolerance of low temperatures, even though that strain displayed the maximum growth index at 20 °C, compared to the 30-35 °C of Asian, African, and South American strains.

    “A draft genome of a cold-resistant spirulina strain obtained from Solenoye Lake in Siberia did not identify any unique genes related to its tolerance of low temperatures, even though that strain displayed the maximum growth index at 20 °C, compared to the 30–35 °C of Asian, African, and South American strains [125].”

    From Spirulina/Arthrospira/Limnospira—Three Names of the Single Organism (2024) · cites this paper as [125]

    Split into 2 atoms — 0 confirmed, 1 partially supported, 1 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.

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  • Several genomes from genus Arthrospira that belong to geographically distinct lineages have been nearly completely recovered by independent sequencing and assembly into single super-scaffolds, including A. platensis NIES-39, Arthrospira sp. PCC 8005 and A. platensis C1.

    “In the past 6 years, several genomes from genus Arthrospira that belong to geographically distinct lineages have been nearly completely recovered by independent sequencing and assembly into single super-scaffolds, respectively, including A. platensis NIES-39, Arthrospira sp. PCC 8005 and A. platensis C1.”

    From Whole genomic DNA sequencing and comparative genomic analysis of<i>Arthrospira platensis</i>: high genome plasticity and genetic diversity (2016) · cites this paper as [6]

    The Genome project history section (page not provided) lists separate sequencing projects for NIES-39, PCC8005, and C1. Genome sequencing and assembly (page not provided) reports one scaffold with 63 gaps for C1, but does not establish single-super-scaffold assemblies for the other two strains. The copy also does not establish that the strains belong to geographically distinct lineages. (LLM, conf=0.85)

    Experimental — accuracy not yet measured
  • Unlike other bacteria, the genome of microorganisms belonging to phylum Cyanobacterium generally possesses a large amount of dispersed repetitive sequences, particularly Arthrospira, thereby causing difficulty in the complete assembly of its genome.

    “Unlike other bacteria, the genome of microorganisms belonging to phylum Cyanobacterium generally possesses a large amount of dispersed repetitive sequences, particularly Arthrospira, thereby causing difficulty in the complete assembly of its genome.”

    From Whole genomic DNA sequencing and comparative genomic analysis of<i>Arthrospira platensis</i>: high genome plasticity and genetic diversity (2016) · cites this paper as [6]

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  • Arthrospira genomes encode NapA-type Na+/H+ antiporter homologs, which can be involved in salt tolerance in alkaline habitats.

    “Arthrospira genomes also encode NapA-type Na+/H+ antiporter homologs, which can be involved in salt tolerance in alkaline habitats 11.”
  • In general, Siberian strains did not differ from tropical strains in terms of the presence of stress response genes.

    “In general, Siberian strains did not differ from tropical strains in terms of the presence of stress response genes.”

    From Spirulina/Arthrospira/Limnospira—Three Names of the Single Organism (2024) · cites this paper as [125]

    The Genomic comparison section compares Arthrospira genomes, and the Insights from the genome sequence section discusses defense-related genes, but neither compares Siberian with tropical strains for stress-response genes. Searches for “Siberian,” “tropical,” and “stress response genes” found no passage addressing that comparison. (LLM, conf=0.76)

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Cites

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Research works printed but not linked: 3

  1. [2]Richmond A. Spirulina, Microalgal Biotechnology. In: Borowitzka M, Borowitzka L, editors. Microalgal Biotechnology. New York: Cambridge University Press; 1987. p. 85-121.
  2. [12]Woese CR Stackebrandt E Macke TJ Fox GE A phylogenetic definition of the major eubacterial taxa. Syst Appl Microbiol 1985; 6: 143- 151 10.1016/S0723-2020(85)80047-3 11542017 · DOI
  3. [19]Zarrouk C. Contribution a` l’e’tude d’une cyanophyce’e. Influence de divers facteurs physiques et chimiques sur la croissance et la photosynthe`se de Spirulina maxima Ph. D. Thesis, Universite´ de Paris. 1966.

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Authors
Cheevadhanarak, S., Paithoonrangsarid, K., Prommeenate, P., Kaewngam, W., Musigkain, A., Tragoonrung, S., Tabata, S., Kaneko, T., Chaijaruwanich, J., Sangsrakru, D., Tangphatsornruang, S., Chanprasert, J., Tongsima, S., Kusonmano, K., Jeamton, W., Dulsawat, S., Klanchui, A., Vorapreeda, T., Chumchua, V., Khannapho, C., Thammarongtham, C., Plengvidhya, V., Subudhi, S., Hongsthong, A., Ruengjitchatchawalya, M., Meechai, A., Senachak, J., & Tanticharoen, M.
Affiliations
  • National Center for Genetic Engineering and Biotechnology (TH)
  • King Mongkut's University of Technology Thonburi (TH)
  • Kazusa DNA Research Institute (JP)
  • Chiang Mai University (TH)
Corresponding author
Cheevadhanarak, Supapon
Venue
Standards in Genomic Sciences
Published
2012-03-05
Volume
6
Issue
1
Pages
43-53
ISSN
1944-3277 (ISSN-L)
OpenAlex
W2133828368
Cited by
59
References
24
Citations by year
2026: 3 · 2025: 1 · 2024: 6 · 2023: 6 · 2022: 4 · 2021: 5 · 2020: 6 · 2019: 5 · 2018: 3 · 2017: 7 · 2016: 3 · 2015: 3 · 2014: 3 · 2013: 1 · 2012: 3
FWCI
1.42
Type
journal article
Language
en
Open access
Locations
  • Standards in Genomic Sciences (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Greater South Information System
Funders
  • Institut de France
  • Ben-Gurion University of the Negev
  • National Center for Genetic Engineering and Biotechnology
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Algal biology and biofuel production
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Photosynthetic Processes and Mechanisms
Keywords
Spirulina platensis, cyanobacteria, genome sequence, genome annotation, protein-coding genes, photosynthetic efficiency, metabolic pathways, Spirulina

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