» Articles » PMID: 21059706

Genome Sequence of Kitasatospora Setae NBRC 14216T: an Evolutionary Snapshot of the Family Streptomycetaceae

Abstract

Kitasatospora setae NBRC 14216(T) (=KM-6054(T)) is known to produce setamycin (bafilomycin B1) possessing antitrichomonal activity. The genus Kitasatospora is morphologically similar to the genus Streptomyces, although they are distinguishable from each other on the basis of cell wall composition and the 16S rDNA sequence. We have determined the complete genome sequence of K. setae NBRC 14216(T) as the first Streptomycetaceae genome other than Streptomyces. The genome is a single linear chromosome of 8,783,278 bp with terminal inverted repeats of 127,148 bp, predicted to encode 7569 protein-coding genes, 9 rRNA operons, 1 tmRNA and 74 tRNA genes. Although these features resemble those of Streptomyces, genome-wide comparison of orthologous genes between K. setae and Streptomyces revealed smaller extent of synteny. Multilocus phylogenetic analysis based on amino acid sequences unequivocally placed K. setae outside the Streptomyces genus. Although many of the genes related to morphological differentiation identified in Streptomyces were highly conserved in K. setae, there were some differences such as the apparent absence of the AmfS (SapB) class of surfactant protein and differences in the copy number and variation of paralogous components involved in cell wall synthesis.

Citing Articles

Genomic and physiological characterization of Kitasatospora sp. nov., an actinobacterium with potential for biotechnological application isolated from Cerrado soil.

Cunha-Ferreira I, Vizzotto C, Freitas M, Peixoto J, Carvalho L, Totola M Braz J Microbiol. 2024; 55(2):1099-1115.

PMID: 38605254 PMC: 11153394. DOI: 10.1007/s42770-024-01324-y.


Phylogenetic Analysis and Characterization of Odorous Compound-Producing Actinomycetes in Sediments in the Sanbe Reservoir, A Drinking Water Reservoir in Japan.

Hayashi S, Masuki S, Furuta K, Doi S, Kim S, Seike Y Curr Microbiol. 2022; 79(11):344.

PMID: 36209310 DOI: 10.1007/s00284-022-03052-8.


Complete Genome Sequence of Two Deep-Sea Isolates from Madeira Archipelago and Evaluation of Their Biosynthetic Potential.

Albuquerque P, Ribeiro I, Correia S, Mucha A, Tamagnini P, Braga-Henriques A Mar Drugs. 2021; 19(11).

PMID: 34822492 PMC: 8622039. DOI: 10.3390/md19110621.


Adaptation to Endophytic Lifestyle Through Genome Reduction by sp. SUK42.

Zin N, Ismail A, Mark D, Westrop G, Schniete J, Herron P Front Bioeng Biotechnol. 2021; 9:740722.

PMID: 34712653 PMC: 8545861. DOI: 10.3389/fbioe.2021.740722.


Phylogenetic analysis of the salinipostin γ-butyrolactone gene cluster uncovers new potential for bacterial signalling-molecule diversity.

Creamer K, Kudo Y, Moore B, Jensen P Microb Genom. 2021; 7(5).

PMID: 33979276 PMC: 8209734. DOI: 10.1099/mgen.0.000568.


References
1.
Nett M, Ikeda H, Moore B . Genomic basis for natural product biosynthetic diversity in the actinomycetes. Nat Prod Rep. 2009; 26(11):1362-84. PMC: 3063060. DOI: 10.1039/b817069j. View

2.
Ishikawa J, Hotta K . FramePlot: a new implementation of the frame analysis for predicting protein-coding regions in bacterial DNA with a high G + C content. FEMS Microbiol Lett. 1999; 174(2):251-3. DOI: 10.1111/j.1574-6968.1999.tb13576.x. View

3.
Laslett D, Canback B . ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences. Nucleic Acids Res. 2004; 32(1):11-6. PMC: 373265. DOI: 10.1093/nar/gkh152. View

4.
Momose I, Sekizawa R, Hirosawa S, Ikeda D, Naganawa H, Iinuma H . Tyropeptins A and B, new proteasome inhibitors produced by Kitasatospora sp. MK993-dF2. II. Structure determination and synthesis. J Antibiot (Tokyo). 2002; 54(12):1004-12. DOI: 10.7164/antibiotics.54.1004. View

5.
Mulder N, Apweiler R, Attwood T, Bairoch A, Bateman A, Binns D . New developments in the InterPro database. Nucleic Acids Res. 2007; 35(Database issue):D224-8. PMC: 1899100. DOI: 10.1093/nar/gkl841. View