Genome sequencing, assembly, and annotation of the self-flocculating microalga Scenedesmus obliquus AS-6-11.
Cell self-flocculation
Comparative genomics
Genome assembly and annotation
Green microalgae
Scenedesmus obliquus
Journal
BMC genomics
ISSN: 1471-2164
Titre abrégé: BMC Genomics
Pays: England
ID NLM: 100965258
Informations de publication
Date de publication:
27 Oct 2020
27 Oct 2020
Historique:
received:
16
07
2020
accepted:
11
10
2020
entrez:
28
10
2020
pubmed:
29
10
2020
medline:
15
5
2021
Statut:
epublish
Résumé
Scenedesmus obliquus belongs to green microalgae and is widely used in aquaculture as feed, which is also explored for lipid production and bioremediation. However, genomic studies of this microalga have been very limited. Cell self-flocculation of microalgal cells can be used as a simple and economic method for harvesting biomass, and it is of great importance to perform genome-scale studies for the self-flocculating S. obliquus strains to promote their biotechnological applications. We employed the Pacific Biosciences sequencing platform for sequencing the genome of the self-flocculating microalga S. obliquus AS-6-11, and used the MECAT software for de novo genome assembly. The estimated genome size of S. obliquus AS-6-11 is 172.3 Mbp with an N50 of 94,410 bp, and 31,964 protein-coding genes were identified. Gene Ontology (GO) and KEGG pathway analyses revealed 65 GO terms and 428 biosynthetic pathways. Comparing to the genome sequences of the well-studied green microalgae Chlamydomonas reinhardtii, Chlorella variabilis, Volvox carteri and Micractinium conductrix, the genome of S. obliquus AS-6-11 encodes more unique proteins, including one gene that encodes D-mannose binding lectin. Genes encoding the glycosylphosphatidylinositol (GPI)-anchored cell wall proteins, and proteins with fasciclin domains that are commonly found in cell wall proteins might be responsible for the self-flocculating phenotype, and were analyzed in detail. Four genes encoding both GPI-anchored cell wall proteins and fasciclin domain proteins are the most interesting targets for further studies. The genome sequence of the self-flocculating microalgal S. obliquus AS-6-11 was annotated and analyzed. To our best knowledge, this is the first report on the in-depth annotation of the S. obliquus genome, and the results will facilitate functional genomic studies and metabolic engineering of this important microalga. The comparative genomic analysis here also provides new insights into the evolution of green microalgae. Furthermore, identification of the potential genes encoding self-flocculating proteins will benefit studies on the molecular mechanism underlying this phenotype for its better control and biotechnological applications as well.
Sections du résumé
BACKGROUND
BACKGROUND
Scenedesmus obliquus belongs to green microalgae and is widely used in aquaculture as feed, which is also explored for lipid production and bioremediation. However, genomic studies of this microalga have been very limited. Cell self-flocculation of microalgal cells can be used as a simple and economic method for harvesting biomass, and it is of great importance to perform genome-scale studies for the self-flocculating S. obliquus strains to promote their biotechnological applications.
RESULTS
RESULTS
We employed the Pacific Biosciences sequencing platform for sequencing the genome of the self-flocculating microalga S. obliquus AS-6-11, and used the MECAT software for de novo genome assembly. The estimated genome size of S. obliquus AS-6-11 is 172.3 Mbp with an N50 of 94,410 bp, and 31,964 protein-coding genes were identified. Gene Ontology (GO) and KEGG pathway analyses revealed 65 GO terms and 428 biosynthetic pathways. Comparing to the genome sequences of the well-studied green microalgae Chlamydomonas reinhardtii, Chlorella variabilis, Volvox carteri and Micractinium conductrix, the genome of S. obliquus AS-6-11 encodes more unique proteins, including one gene that encodes D-mannose binding lectin. Genes encoding the glycosylphosphatidylinositol (GPI)-anchored cell wall proteins, and proteins with fasciclin domains that are commonly found in cell wall proteins might be responsible for the self-flocculating phenotype, and were analyzed in detail. Four genes encoding both GPI-anchored cell wall proteins and fasciclin domain proteins are the most interesting targets for further studies.
CONCLUSIONS
CONCLUSIONS
The genome sequence of the self-flocculating microalgal S. obliquus AS-6-11 was annotated and analyzed. To our best knowledge, this is the first report on the in-depth annotation of the S. obliquus genome, and the results will facilitate functional genomic studies and metabolic engineering of this important microalga. The comparative genomic analysis here also provides new insights into the evolution of green microalgae. Furthermore, identification of the potential genes encoding self-flocculating proteins will benefit studies on the molecular mechanism underlying this phenotype for its better control and biotechnological applications as well.
Identifiants
pubmed: 33109102
doi: 10.1186/s12864-020-07142-4
pii: 10.1186/s12864-020-07142-4
pmc: PMC7590803
doi:
Substances chimiques
Glycolates
0
4-O-carboxymethylascochlorin
I1BK0ZE06X
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
743Références
Bioresour Technol. 2011 Jan;102(1):71-81
pubmed: 20674344
J Bacteriol. 1997 Aug;179(15):4929-36
pubmed: 9244284
Biotechnol Adv. 2009 Nov-Dec;27(6):849-856
pubmed: 19577627
Nature. 2012 Aug 16;488(7411):329-35
pubmed: 22895338
Bioinformatics. 2015 Oct 1;31(19):3210-2
pubmed: 26059717
Biotechnol J. 2016 Mar;11(3):336-44
pubmed: 26849021
Nat Methods. 2017 Nov;14(11):1072-1074
pubmed: 28945707
BMC Genomics. 2014 Mar 19;15:212
pubmed: 24646409
Biotechnol J. 2017 Nov;12(11):
pubmed: 28865139
Bioresour Technol. 2020 Apr;302:122903
pubmed: 32018084
BMC Bioinformatics. 2004 May 14;5:59
pubmed: 15144565
Biotechnol Adv. 2020 Nov 1;43:107554
pubmed: 32437732
iScience. 2019 Jan 25;11:450-465
pubmed: 30684492
Bioinformatics. 2005 May 1;21(9):1846-52
pubmed: 15691858
Bioinformatics. 2008 Mar 1;24(5):637-44
pubmed: 18218656
Biotechnol Biofuels. 2018 Nov 9;11:308
pubmed: 30455737
Bioresour Technol. 2013 Oct;145:285-9
pubmed: 23419992
Bioinformatics. 2014 May 1;30(9):1236-40
pubmed: 24451626
BMC Bioinformatics. 2011 Dec 22;12:491
pubmed: 22192575
Genome Res. 2000 Jun;10(6):819-31
pubmed: 10854413
J Fungi (Basel). 2018 May 17;4(2):
pubmed: 29772751
Appl Microbiol Biotechnol. 2019 Apr;103(7):3085-3097
pubmed: 30737536
Yeast. 1998 Jan 15;14(1):25-35
pubmed: 9483793
J Appl Phycol. 2011 Oct;23(5):849-855
pubmed: 21957329
Bioresour Technol. 2013 Oct;145:142-9
pubmed: 23566474
J Biosci Bioeng. 2014 Jul;118(1):29-33
pubmed: 24507901
Front Microbiol. 2020 May 07;11:792
pubmed: 32457714
New Phytol. 2015 Jun;206(4):1314-27
pubmed: 25676073
BMC Genomics. 2017 Mar 9;18(1):223
pubmed: 28274201
Yeast. 2000 Jan 30;16(2):99-110
pubmed: 10641033
Sci Rep. 2019 Aug 1;9(1):11200
pubmed: 31371830
EMBO J. 1994 Sep 15;13(18):4212-22
pubmed: 7925267
Int J Mol Sci. 2018 May 31;19(6):
pubmed: 29857505
Nucleic Acids Res. 2015 Jul 1;43(W1):W78-84
pubmed: 25964301
J Hazard Mater. 2019 Aug 5;375:115-120
pubmed: 31054528
Plant Cell Physiol. 2013 Jul;54(7):1027-40
pubmed: 23737502
Genome Announc. 2017 Aug 10;5(32):
pubmed: 28798164
Bioresour Technol. 2017 Apr;229:53-62
pubmed: 28107722
Bioresour Technol. 2015 May;184:251-257
pubmed: 25499148
Nucleic Acids Res. 1997 Sep 1;25(17):3389-402
pubmed: 9254694
Mol Biol Evol. 2016 Jul;33(7):1870-4
pubmed: 27004904
Genomics Proteomics Bioinformatics. 2015 Oct;13(5):278-89
pubmed: 26542840
Genome Announc. 2017 Jan 19;5(3):
pubmed: 28104651
Biotechnol Bioeng. 2018 Nov;115(11):2714-2725
pubmed: 30063083
Plant Physiol. 2002 Jun;129(2):486-99
pubmed: 12068095
mBio. 2015 Apr 14;6(2):
pubmed: 25873380
BMC Genomics. 2018 Oct 22;19(1):765
pubmed: 30348078
J Biotechnol. 2014 Mar 20;174:34-8
pubmed: 24480568