Whole genome sequence analysis of Geitlerinema sp. FC II unveils competitive edge of the strain in marine cultivation system for biofuel production
A filamentous cyanobacteria, Geitlerinema sp. FC II, was isolated from marine algae culture pond at Reliance Industries Limited (RIL), India. The 6.7 Mb draft genome of FC II encodes for 6697 protein coding genes. Analysis of the whole genome sequence revealed presence of nif gene cluster, supportin...
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Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 2019-05, Vol.111 (3), p.465-472 |
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Zusammenfassung: | A filamentous cyanobacteria, Geitlerinema sp. FC II, was isolated from marine algae culture pond at Reliance Industries Limited (RIL), India. The 6.7 Mb draft genome of FC II encodes for 6697 protein coding genes. Analysis of the whole genome sequence revealed presence of nif gene cluster, supporting its capability to fix atmospheric nitrogen. FC II genome contains two variants of sulfide:quinone oxidoreductases (SQR), which is a crucial elector donor in cyanobacterial metabolic processes. FC II is characterized by the presence of multiple CRISPR- Cas (Clustered Regularly Interspaced Short Palindrome Repeats – CRISPR associated proteins) clusters, multiple variants of genes encoding photosystem reaction centres, biosynthetic gene clusters of alkane, polyketides and non-ribosomal peptides. Presence of these pathways will help FC II in gaining an ecological advantage over other strains for biomass production in large scale cultivation system. Hence, FC II may be used for production of biofuel and other industrially important metabolites.
•Filamentous-cyabobacterium, FCII, isolated from raceway pond of biofuel facility.•6.7 Mb draft genome of FC II has 53% GC and encodes for 6697 protein coding genes.•FC II has 3 variants of psaA and 2 of psaK gene of photosystem reaction centre.•Presence of terminal acceptors CoxBAC indicates its ability to grow heterotropically.•Multiple CRISPR-Cas clusters provide a form of heritable adaptive immunity. |
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ISSN: | 0888-7543 1089-8646 |
DOI: | 10.1016/j.ygeno.2018.03.004 |