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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/02/17 05:44:35」(JST)

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1. 駆虫薬療法 anthelminthic therapies
2. ノカルジア症の微生物学、疫学、および病因 microbiology epidemiology and pathogenesis of nocardiosis
3. 心臓移植における免疫抑制療法の導入および維持 induction and maintenance of immunosuppressive therapy in cardiac transplantation
4. 移植片対宿主病の予防および治療に使用される免疫抑制剤の概要 overview of immunosuppressive agents used for prevention and treatment of graft versus host disease
5. マイトマイシン-Cの肺毒性 mitomycin c pulmonary toxicity

Structure and Activity of NADPH-Dependent Reductase Q1EQE0 from Streptomyces kanamyceticus, which Catalyses the R-Selective Reduction of an Imine Substrate.

Rodríguez-Mata M, Frank A, Wells E, Leipold F, Turner NJ, Hart S, Turkenburg JP, Grogan G.SourceYork Structural Biology Laboratory, Department of Chemistry, University of York, Heslington, York, YO10 5DD (UK); Universidad de Oviedo, Facultad de Química, Química Orgánica e Inorgánica, Julian Clavería 8, C.P. 33006 Oviedo, Asturias (Spain).
Chembiochem : a European journal of chemical biology.Chembiochem.2013 Jul 22;14(11):1372-9. doi: 10.1002/cbic.201300321. Epub 2013 Jun 28.
NADPH-dependent oxidoreductase Q1EQE0 from Streptomyces kanamyceticus catalyzes the asymmetric reduction of the prochiral monocyclic imine 2-methyl-1-pyrroline to the chiral amine (R)-2-methylpyrrolidine with >99 % ee, and is thus of interest as a potential biocatalyst for the production of opt
PMID 23813853

Discovery of parallel pathways of kanamycin biosynthesis allows antibiotic manipulation.

Park JW, Park SR, Nepal KK, Han AR, Ban YH, Yoo YJ, Kim EJ, Kim EM, Kim D, Sohng JK, Yoon YJ.SourceDepartment of Chemistry and Nanoscience, Ewha Womans University, Seoul, Republic of Korea.
Nature chemical biology.Nat Chem Biol.2011 Oct 9;7(11):843-52. doi: 10.1038/nchembio.671.
Kanamycin is one of the most widely used antibiotics, yet its biosynthetic pathway remains unclear. Current proposals suggest that the kanamycin biosynthetic products are linearly related via single enzymatic transformations. To explore this system, we have reconstructed the entire biosynthetic path
PMID 21983602

A system for the targeted amplification of bacterial gene clusters multiplies antibiotic yield in Streptomyces coelicolor.

Murakami T, Burian J, Yanai K, Bibb MJ, Thompson CJ.SourceDepartment of Microbiology and Immunology, University of British Columbia, Vancouver, BC, Canada, V6T 1Z3.
Proceedings of the National Academy of Sciences of the United States of America.Proc Natl Acad Sci U S A.2011 Sep 20;108(38):16020-5. doi: 10.1073/pnas.1108124108. Epub 2011 Sep 8.
Gene clusters found in bacterial species classified as Streptomyces encode the majority of known antibiotics as well as many pharmaceutically active compounds. A site-specific recombination system similar to those that mediate plasmid conjugation was engineered to catalyze tandem amplification of on
PMID 21903924

Biosynthetic approach for the production of new aminoglycoside derivative(BIOCHEMICAL ENGINEERING)

Phylogenetic Analysis of Immunosuppressant FK506-Producing Streptomycete Strains

Journal of antibiotics = An International Journal Devoted to Research on Bioactive Microbial Products 57(5), 351-354, 2004-05-25
NAID 10012927932

Streptomyces kanamyceticus
Scientific classification
Kingdom:	Bacteria
Phylum:	Actinobacteria
Class:	Actinobacteria
Order:	Actinomycetales
Family:	Streptomycetaceae
Genus:	Streptomyces
Species:	S. kanamyceticus
Binomial name
	Streptomyces kanamyceticus;