Research Topics
Genomes and Genes | S OmuraSummaryAffiliation: The Kitasato Institute Country: Japan Publications
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Publications
EM703 improves bleomycin-induced pulmonary fibrosis in mice by the inhibition of TGF-beta signaling in lung fibroblastsYing Ji Li
Fourth Department of Internal Medicine, Nippon Medical School, Tokyo, Japan
Respir Res 7:16. 2006..We investigated the anti-inflammatory and antifibrotic effects of EM703 in an experimental model of bleomycin-induced lung injury and subsequent fibrosis in mice...
An anthelmintic compound, nafuredin, shows selective inhibition of complex I in helminth mitochondriaS Omura
Research Center for Biological Function, The Kitasato Institute, Shirokane, Minato ku, Tokyo 108 8642, Japan
Proc Natl Acad Sci U S A 98:60-2. 2001..Thus, our study indicates that mitochondrial complex I is a promising target for chemotherapy, and nafuredin is a potential lead compound as an anthelmintic isolated from microorganisms...
Genome sequence of an industrial microorganism Streptomyces avermitilis: deducing the ability of producing secondary metabolitesS Omura
The Kitasato Institute for Life Sciences, Kitasato University, Tokyo 108 8642, Japan
Proc Natl Acad Sci U S A 98:12215-20. 2001..These secondary metabolite clusters are widely located in the genome but half of them are near both ends of the genome. The total length of these clusters occupies about 6.4% of the genome...
The life and times of ivermectin - a success storySatoshi Omura
Kitasato Institute, 5 9 1 Shirokane, Minato ku, Tokyo 108 8642, Japan
Nat Rev Microbiol 2:984-9. 2004..The drug is now being used, free of charge, in two global disease-elimination programmes that are benefiting millions of the world's poorest people...
Ivermectin: 25 years and still going strongS Omura
The Kitasato Institute, Tokyo, Japan
Int J Antimicrob Agents 31:91-8. 2008....
Nafuredin, a novel inhibitor of NADH-fumarate reductase, produced by Aspergillus niger FT-0554H Ui
Research Center for Biological Function, The Kitasato Institute, Tokyo, Japan
J Antibiot (Tokyo) 54:234-8. 2001..It was obtained from culture broth of Aspergillus niger FT-0554 isolated from a marine sponge. The structure was elucidated as an epoxy-delta-lactone with an attached methylated olefinic side chain on the basis of spectral analysis...
Total synthesis of nafuredin, a selective NADH-fumarate reductase inhibitorD Takano
School of Pharmaceutical Science, Kitasato University, Kitasato Institute for Life Sciences, Kitasato University, and CREST, The Japan Science and Technology Corporation (JST, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan
Org Lett 3:2289-91. 2001..The C1-C8 and C9-C18 segments were derived efficiently from D-glucose and (S)-(-)-2-methyl-1-butanol, respectively, coupled by stereoselective Julia olefination, and converted to nafuredin...
Cloning of the gene encoding avermectin B 5-O-methyltransferase in avermectin-producing Streptomyces avermitilisH Ikeda
School of Pharmaceutical Sciences, Kitasato University, Minato ku, Tokyo 108, Japan
Gene 206:175-80. 1998..Sequence analysis of the aveD region of the mutant strain revealed that a point mutation is within ORF, being Thr23-->Ile substitution. This mutation causes the inactivation of O-methyltransferase activity of AveD...
Deacetylravidomycin M, a new inhibitor of IL-4 signal transduction, produced by Streptomyces sp. WK-6326. II. Structure elucidationM Arai
The Kitasato Institute, Kitasato University, Tokyo, Japan
J Antibiot (Tokyo) 54:562-6. 2001....
Organization of biosynthetic gene cluster for avermectin in Streptomyces avermitilis: analysis of enzymatic domains in four polyketide synthasesH Ikeda
School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan
J Ind Microbiol Biotechnol 27:170-6. 2001..AVES1 and 2 contain two and four modules, respectively, whereas AVES 3 and AVES 4 each contains three modules. The 12 modules correspond to the 12 cycles required for synthesis of the avermectin aglycon...
Cladospolide D, a new 12-membered macrolide antibiotic produced by Cladosporium sp. FT-0012H Zhang
The Kitasato Institute, Tokyo, Japan
J Antibiot (Tokyo) 54:635-41. 2001..The structure of cladospolide D was deduced to be (E)-2-dodecen-5-hydroxy-11-olide-4-one. Cladospolide D showed antifungal activity against Pyricularia oryzae and Mucor racemosus...
Deacetylravidomycin M, a new inhibitor of IL-4 signal transduction, produced by Streptomyces sp. WK-6326. I. Taxonomy, fermentation, isolation and biological activitiesM Arai
The Kitasato Institute, Kitasato University, Tokyo, Japan
J Antibiot (Tokyo) 54:554-61. 2001..Deacetylravidomycin M inhibited IL-4-induced CD23 expression in U937 cells without any cytotoxic effect, whereas deacetylravidomycin showed no inhibitory activity...
A quinol peroxidase inhibitor prevents secretion of a leukotoxin from Aggregatibacter actinomycetemcomitansE Takashima
Department of Microbiology, School of Life Dentistry at Tokyo, The Nippon Dental University, Chiyoda ku, Tokyo, Japan
J Periodontal Res 45:123-8. 2010..In the present study, we aimed to find a highly potent QPO inhibitor to attenuate the virulence of A. actinomycetemcomitans...
Organization of the biosynthetic gene cluster for the polyketide anthelmintic macrolide avermectin in Streptomyces avermitilisH Ikeda
School of Pharmaceutical Sciences, Kitasato University, Tokyo 108 8641, Japan
Proc Natl Acad Sci U S A 96:9509-14. 1999....
Potent antimalarial activities of polyether antibiotic, X-206K Otoguro
Research Center for Tropical Diseases, Research Center for Biological Function, The Kitasato Institute, Tokyo, Japan
J Antibiot (Tokyo) 54:658-63. 2001..These observations are the first report of antimalarial activity of X-206...
Structure-specific inhibition of cholesteryl ester transfer protein by azaphilonesH Tomoda
Research Center for Biological Function, The Kitasato Institute, Tokyo, Japan
J Antibiot (Tokyo) 52:160-70. 1999..4 and 10.3 microM, respectively). A model of the reaction suggested that sclerotiorin reacts with a primary amine of amino acids such as lysine in the protein to form a covalent bond...
Description of two novel species of the genus Kitasatospora Omura et al. 1982, Kitasatospora cineracea sp. nov. and Kitasatospora niigatensis sp. novK Tajima
Research Center for Biological Function, The Kitasato Institute, Tokyo, Japan
Int J Syst Evol Microbiol 51:1765-71. 2001..nov. and Kitasatospora niigatensis sp. nov., with the type strains K. cineracea SK-3255T (= IFO 16452T = JCM 10915T = NRRL B-23134T) and K. niigatensis SK-3406T (= IFO 16453T = JCM 10916T = NRRL B-24135T)...
Satoshi Omura: in pursuit of nature's bountyAndy Crump
Research Centre for Tropical Diseases, The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8642, Japan
Trends Parasitol 21:126-32. 2005..It has also improved the health of pets and livestock around the globe, and encouraged development of a community-based delivery mechanism that could herald a revolution in public health care in Africa...
Streptomyces avermectinius sp. nov., an avermectin-producing strainYoko Takahashi
Kitasato Institute for Life Sciences, Kitasato University, 5-9-1, Shirokane, Minato-ku, Tokyo 108-8641, Japan
Int J Syst Evol Microbiol 52:2163-8. 2002..Analysis of DNA-DNA hybridization tests distinguished strain MA-4680(T) from these eight Streptomyces species. The type strain is strain MA-4680(T) (= ATCC 31267(T) = NRRL 8165(T))...
Erythromycin suppresses nuclear factor-kappaB and activator protein-1 activation in human bronchial epithelial cellsM Desaki
Department of Respiratory Medicine, University of Tokyo Graduate School of Medicine, Tokyo, Japan
Biochem Biophys Res Commun 267:124-8. 2000..Our findings support the concept that the recruitment of neutrophils in airway diseases may be regulated by NF-kappaB and AP-1...
Molecular cloning of actinohivin, a novel anti-HIV protein from an actinomycete, and its expression in Escherichia coliJ Inokoshi
School of Pharmaceutical Sciences, Kitasato University, Shirokane, Minato-ku, Tokyo, 108-8641, Japan
Biochem Biophys Res Commun 281:1261-5. 2001..The actinohivin gene could be expressed in E. coli using a pET30Xa/LIC expression vector and the purified recombinant actinohivin was found to inhibit syncytium formation to a similar extent as actinohivin from its natural source...
Chlorogentisylquinone, a new neutral sphingomyelinase inhibitor, produced by a marine fungusR Uchida
Kitasato Institute for Life Sciences, Kitasato University and The Kitasato Institute, Tokyo, Japan
J Antibiot (Tokyo) 54:882-9. 2001..Chlorogentisylquinone inhibited neutral sphingomyelinase activity of rat brain membranes with an IC50 value of 1.2 microM...
Hygromycin A, an antitreponemal substance. II. Therapeutic effect for swine dysenteryA Nakagawa
Kitasato Institute, School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan
J Antibiot (Tokyo) 40:1627-35. 1987..T. hyodysenteriae-caused swine dysentery was successfully controlled by feeding hygromycin A at 5 g/ton. Hygromycin A medicated pigs performed as well as or better than carbadox-medicated pigs...
Nosokomycins, new antibiotics discovered in an in vivo-mimic infection model using silkworm larvae. I: Fermentation, isolation and biological propertiesRyuji Uchida
Graduate School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan
J Antibiot (Tokyo) 63:151-5. 2010..Nosokomycins inhibited the growth of MRSA with MIC values of 0.125 microg ml(-1) using the liquid microdilution method. Furthermore, MRSA-infected silkworms survived when nosokomycin A or B was injected at a dose of 50 microg per larva...
Sinefungin VA and dehydrosinefungin V, new antitrypanosomal antibiotics produced by Streptomyces sp. K05-0178Megumi Niitsuma
Research Center for Tropical Diseases, Kitasato Institute for Life Sciences, Kitasato University, Tokyo, Japan
J Antibiot (Tokyo) 63:673-9. 2010..0026 μg ml(-1) in vitro without cytotoxicity against MRC-5 cells. Dehydrosinefungin V showed moderate antitrypanosomal activity (IC(50)=0.15 μg ml(-1))...
Decursin and decursinol angelate selectively inhibit NADH-fumarate reductase of Ascaris suumKazuro Shiomi
Kitasato Institute for Life Sciences, Kitasato University, Tokyo, Japan
Planta Med 73:1478-81. 2007..In contrast, decursinol angelate moderately inhibits bovine heart complexes II and III. Decursinol inhibits A. SUUM NFRD to a similar extent, but its target is complex II. It also inhibits bovine heart complexes II and III...
Cyslabdan, a new potentiator of imipenem activity against methicillin-resistant Staphylococcus aureus, produced by Streptomyces sp. K04-0144. I. Taxonomy, fermentation, isolation and structural elucidationAtsushi Fukumoto
Kitasato Institute for Life Sciences and Graduate School of Infection Control Sciences, Kitasato University, 5 9 1 Shirokane, Minato ku, Tokyo, Japan
J Antibiot (Tokyo) 61:1-6. 2008..The structure of cyslabdan was elucidated by spectroscopic analyses including NMR. The compound has a labdane-type diterpene skeleton connecting with an N-acetylcysteine via thioether linkage...
Cyslabdan, a new potentiator of imipenem activity against methicillin-resistant Staphylococcus aureus, produced by Streptomyces sp. K04-0144. II. Biological activitiesAtsushi Fukumoto
Kitasato Institute for Life Sciences and Graduate School of Infection Control Sciences, Kitasato University, 5 9 1 Shirokane, Minato ku, Tokyo, Japan
J Antibiot (Tokyo) 61:7-10. 2008..Furthermore, among beta-lactam antibiotics, the activity of carbapenems was most remarkably potentiated by cyslabdan...
Guadinomines, Type III secretion system inhibitors, produced by Streptomyces sp. K01-0509. I: taxonomy, fermentation, isolation and biological propertiesMasato Iwatsuki
The Kitasato Institute, Japan
J Antibiot (Tokyo) 61:222-9. 2008..Guadinomines A and B showed potent inhibition with IC50 values of 0.02 and 0.007 microg/ml, respectively, guadinomine D showed moderate activity (IC50: 8.5 microg/ml), while guadinomines C1 and C2 and guadinomic acid had no activity...
Anti-atherosclerotic activity of triacsin C, an acyl-CoA synthetase inhibitorDaisuke Matsuda
School of Pharmacy, Kitasato University, Shirokane, Tokyo, Japan
J Antibiot (Tokyo) 61:318-21. 2008..The results strongly suggested that triacsin C shows anti-atherogenic activity by inhibiting acyl-CoA synthetase activity...
Nosokomycins, new antibiotics discovered in an in vivo-mimic infection model using silkworm larvae. II: Structure elucidationRyuji Uchida
Graduate School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan
J Antibiot (Tokyo) 63:157-63. 2010..All nosokomycins lack the cyclopentenone moiety in the oligosaccharide moiety of moenomycin A...
Genome-minimized Streptomyces host for the heterologous expression of secondary metabolismMamoru Komatsu
Laboratory of Microbial Engineering, Kitasato Institute for Life Sciences, Kitasato University, 1 15 1 Kitasato Sagamihara, Kanagawa 228 8555, Japan
Proc Natl Acad Sci U S A 107:2646-51. 2010..These findings highlight the strength and flexibility of engineered S. avermitilis as a model host for heterologous gene expression, resulting in the production of exogenous natural and unnatural metabolites...
Phenatic acids A and B, new potentiators of antifungal miconazole activity produced by Streptomyces sp. K03-0132Takashi Fukuda
Kitasato Institute for Life Sciences and Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan
J Antibiot (Tokyo) 58:252-9. 2005..These compounds potentiate miconazole activity against Candida albicans. Phenatic acid B also showed moderate antimicrobial activity against Bacillus subtilis, Staphylococcus aureus, Bacteroides fragilis and Acholeplasma laidlawii...
A new antibiotic, antimycin Ag, produced by Streptomyces sp. K01-0031Kazuro Shiomi
School of Pharmaceutical Sciences, Kitasato University, Minato ku, Tokyo 108 8641, Japan
J Antibiot (Tokyo) 58:74-8. 2005..It showed potent nematocidal and insecticidal activities against Caenorhabditis elegans and Artemia salina, respectively. It inhibited bovine heart NADH oxidase at nanomolar level like other known antimycins...
A gamma-lactone form nafuredin, nafuredin-gamma, also inhibits helminth complex IKazuro Shiomi
School of Pharmaceutical Sciences, Kitasato University, Minato ku, Tokyo 108 8641, Japan
J Antibiot (Tokyo) 58:50-5. 2005..Nafuredin-gamma shows similar complex I inhibitory activity as nafuredin, and it also possesses anthelmintic activity in vivo...
Total synthesis of (-)-borrelidinTohru Nagamitsu
School of Pharmaceutical Science, Kitasato University, Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan
Org Lett 6:1865-7. 2004..Et(2)O-mediated chelation-controlled allylation. [reaction: see text]..
Complete genome sequence and comparative analysis of the industrial microorganism Streptomyces avermitilisHaruo Ikeda
Kitasato Institute for Life Sciences, Kitasato University, Kanagawa 228-8555, Japan
Nat Biotechnol 21:526-31. 2003..In contrast, the terminal regions were not conserved and preferentially contained nonessential genes...
Guadinomines, Type III secretion system inhibitors, produced by Streptomyces sp. K01-0509. II: physico-chemical properties and structure elucidationMasato Iwatsuki
The Kitasato Institute, Japan
J Antibiot (Tokyo) 61:230-6. 2008....
Streptomyces scabrisporus sp. novXu Ping
Research Center for Biological Function, The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8642, Japan
Int J Syst Evol Microbiol 54:577-81. 2004..On the basis of genomic and physiological properties, the novel species Streptomyces scabrisporus sp. nov. is proposed; the type strain is strain KM-4927(T) (=JCM 11712(T)=NRRL B-24202(T))...
Synthesis and biological activities of novel 4"-alkylidene avermectin derivativesKenichiro Nagai
Kitasato Institute for Life Sciences and Graduate School of Infection Control Sciences, Kitasato University and The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan
Bioorg Med Chem Lett 13:3943-6. 2003..Further modifications led to derivatives bearing diverse functional groups. The new avermectin derivatives showed potent growth inhibitory activity against Artemia salina and Caenorhabditis elegans...
Acylated pregnane glycosides from Caralluma tuberculata and their antiparasitic activityEssam Abdel-Sattar
Department of Natural Products and Alternative Medicine, Faculty of Pharmacy, King Abdulaziz University, Jeddah 21589, Saudi Arabia
Phytochemistry 69:2180-6. 2008..All the isolated compounds were tested for their antimalarial and antitrypanosomal activities as well as their cytotoxicity against human diploid embryonic cell line (MRC5)...
Lanopylins A1, B1, A2 and B2, novel lanosterol synthase inhibitors from Streptomyces sp. K99-5041Yuichi Sakano
Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
J Antibiot (Tokyo) 56:817-26. 2003..These compounds inhibited recombinant human lanosterol synthase with IC50 values of 15, 18, 33, and 41 microM, respectively...
Cytochrome p450 complement (CYPome) of the avermectin-producer Streptomyces avermitilis and comparison to that of Streptomyces coelicolor A3(2)David C Lamb
Institute of Biological Sciences, University of Wales Aberystwyth, Aberystwyth, UK
Biochem Biophys Res Commun 307:610-9. 2003..Amongst this range of CYPs are forms associated with avermectin, filipin, geosmin, and pentalenolactone biosynthesis as well as unknown pathways of secondary metabolism...
Takanawaenes, novel antifungal antibiotics produced by Streptomyces sp. K99-5278. I. Taxonomy, fermentation, isolation and biological propertiesYong-Pil Kim
Kitasato Institute for Life Sciences, Kitasato University and The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan
J Antibiot (Tokyo) 56:448-53. 2003..K99-5278 by solvent extraction, silica-gel column chromatography and HPLC. Takanawaenes showed antifungal activity against Aspergillus niger, Mucor racemosus, Candida albicans and Saccharomyces cerevisiae...
[The genome sequence of soil bacterium Streptomyces]Haruo Ikeda
Tanpakushitsu Kakusan Koso 47:1845-50. 2002
Synthesis and biological evaluation of novel 4"-alkoxy avermectin derivativesKenichiro Nagai
Kitasato Institute for Life Sciences and Graduate School of Infection Control Sciences, Kitasato University and The Kitasato Institute, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan
Bioorg Med Chem Lett 14:4135-9. 2004..Novel 4"-alkoxy avermectin derivatives were synthesized via rhodium carbenoid mediated O-H insertion reaction and tested for antiparasite activity against Artemia salina and Caenorhabditis elegans...
In vitro and in vivo antimalarial activities of a carbohydrate antibiotic, prumycin, against drug-resistant strains of PlasmodiaKazuhiko Otoguro
J Antibiot (Tokyo) 57:400-2. 2004
Studies on terpenoids produced by actinomycetes: oxaloterpins A, B, C, D, and E, diterpenes from Streptomyces sp. KO-3988Keiichiro Motohashi
Faculty of Applied Bioscience, Tokyo University of Agriculture, Tokyo 156 8502, Japan
J Nat Prod 70:1712-7. 2007..The absolute configuration of oxaloterpin A was determined by the modified Mosher's method as 3 R, 5 S, 8 S, 10 R, 13 S...
A gene cluster for biosynthesis of the sesquiterpenoid antibiotic pentalenolactone in Streptomyces avermitilisCharles N Tetzlaff
Department of Chemistry, Brown University, Box H, Providence, Rhode Island 02912-9108, USA
Biochemistry 45:6179-86. 2006..Furthermore, a second GAPDH isozyme (gap2, SAV6296) has been expressed in E. coli and shown to be inactivated by pentalenolactone...
Pentalenolactone biosynthesis. Molecular cloning and assignment of biochemical function to PtlH, a non-heme iron dioxygenase of Streptomyces avermitilisZheng You
Department of Chemistry, Brown University, Box H, Providence, Rhode Island 02912 9108, USA
J Am Chem Soc 128:6566-7. 2006..The steady-state kinetic parameters were kcat = 4.2 +/- 0.6 s-1 and Km (5) = 0.57 +/- 0.19 mM. 8 is a new intermediate in the conversion of the sesquiterpene pentalenene (3) to pentalenolactone (1)...
Isolation and identification of three new 5-alkenyl-3,3(2H)-furanones from two streptomyces species using a genomic screening approachArjun H Banskota
Ecopia BioSciences Inc, 7290 Frederick Banting, Montreal, Quebec, H4S 2A1, Canada
J Antibiot (Tokyo) 59:168-76. 2006..All three new compounds were tested for their electron transport inhibitory activities. They had IC50 values of 1-4 microg/ml against Ascaris suum NADH-fumarate reductase and 1-12 microg/ml against bovine heart NADH oxidase...
Pentalenolactone biosynthesis. Molecular cloning and assignment of biochemical function to PtlI, a cytochrome P450 of Streptomyces avermitilisRichard Quaderer
Department of Chemistry, Brown University, Box H, Providence, Rhode Island 02912-9108, USA
J Am Chem Soc 128:13036-7. 2006..The steady-state kinetic parameters for the oxidation of pentalenene (3) to pentalen-13-ol (6) were kcat = 0.503 +/- 0.006 min-1 and Km = 3.33+/-0.62 muM for 3...
Geosmin biosynthesis in Streptomyces avermitilis. Molecular cloning, expression, and mechanistic study of the germacradienol/geosmin synthaseDavid E Cane
Department of Chemistry, Brown University, Box H, Providence, Rhode Island 02912 9108, USA
J Antibiot (Tokyo) 59:471-9. 2006....
Asymmetric total synthesis of (+)-K01-0509 B: determination of absolute configurationSatoshi Tsuchiya
Kitasato Institute for Life Sciences, Graduate School of Infection Control Sciences, Minato-ku, Tokyo 108-8641, Japan
Org Lett 8:5577-80. 2006..These reactions allowed the cyclic guanidine and the adjacent hydroxy group to be assembled, facilitating the asymmetric total synthesis and determination of the absolute stereochemistry of K01-0509 B. [reaction: see text]...
Pentalenolactone biosynthesis: Molecular cloning and assignment of biochemical function to PtlF, a short-chain dehydrogenase from Streptomyces avermitilis, and identification of a new biosynthetic intermediateZheng You
Department of Chemistry, Brown University, Box H, Providence, RI 02912 9108, USA
Arch Biochem Biophys 459:233-40. 2007..0 in the physiological pH range, while a significant activity enhancement was observed from pH 9.0 to 11.3. At pH 8.0, PtlF had a k(cat) of 0.65+/-0.03 s(-1), with a K(m) for 9 of 6.5+/-1.5 microM and K(m) for NAD(+) of 25+/-3 microM...
Advances in drug discovery and biochemical studiesKiyoshi Kita
Department of Biomedical Chemistry, Graduate School of Medicine, The University of Tokyo, Tokyo 113 0033, Japan
Trends Parasitol 23:223-9. 2007..Intensive studies of parasite energy metabolism, such as NADH-fumarate reductase systems and the synthetic pathways of nucleic acids and amino acids, also contribute to the identification of novel and unique drug targets...
Hyper-inducible expression system for streptomycetesSachio Herai
Institute of Applied Biochemistry and Graduate School of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8572, Japan
Proc Natl Acad Sci U S A 101:14031-5. 2004..Furthermore, the system functioned in important streptomycete strains. Thus, the P(nitA)-NitR system should be a powerful tool for improving the productivity of various useful products in streptomycetes...
Crystal structure of the non-heme iron dioxygenase PtlH in pentalenolactone biosynthesisZheng You
Department of Chemistry, Brown University, Providence, Rhode Island 02912 9108, USA
J Biol Chem 282:36552-60. 2007....
