Relevant bibliographies by topics / Streptomyces cattleya

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Streptomyces cattleya'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Streptomyces cattleya"

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Coyne, Vernon E., and Ralph Kirby. "VC11: an Actinophage Virulent to Streptomyces cattleya and Streptomyces olivaceus." Intervirology 25, no. 2 (1986): 61–68. http://dx.doi.org/10.1159/000149657.

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Hsiao, Nai-hua, and Ralph Kirby. "Comparative genomics of Streptomyces avermitilis, Streptomyces cattleya, Streptomyces maritimus and Kitasatospora aureofaciens using a Streptomyces coelicolor microarray system." Antonie van Leeuwenhoek 93, no. 1-2 (2007): 1–25. http://dx.doi.org/10.1007/s10482-007-9175-1.

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Reid, K. A., R. D. Bowden, L. Dasaradhi, M. R. Amin, and D. B. Harper. "Biosynthesis of fluorinated secondary metabolites by Streptomyces cattleya." Microbiology 141, no. 6 (1995): 1385–93. http://dx.doi.org/10.1099/13500872-141-6-1385.

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Deng, Hai, David O'Hagan, and Christoph Schaffrath. "Fluorometabolite biosynthesis and the fluorinase from Streptomyces cattleya." Natural Product Reports 21, no. 6 (2004): 773. http://dx.doi.org/10.1039/b415087m.

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O’Hagan, David. "Recent developments on the fluorinase from Streptomyces cattleya." Journal of Fluorine Chemistry 127, no. 11 (2006): 1479–83. http://dx.doi.org/10.1016/j.jfluchem.2006.09.006.

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Murphy, Cormac D., Steven J. Moss, and David O'Hagan. "Isolation of an Aldehyde Dehydrogenase Involved in the Oxidation of Fluoroacetaldehyde to Fluoroacetate inStreptomyces cattleya." Applied and Environmental Microbiology 67, no. 10 (2001): 4919–21. http://dx.doi.org/10.1128/aem.67.10.4919-4921.

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ABSTRACT Streptomyces cattleya is unusual in that it produces fluoroacetate and 4-fluorothreonine as secondary metabolites. We now report the isolation of an NAD+-dependent fluoroacetaldehyde dehydrogenase from S. cattleya that mediates the oxidation of fluoroacetaldehyde to fluoroacetate. This is the first enzyme to be identified that is directly involved in fluorometabolite biosynthesis. Production of the enzyme begins in late exponential growth and continues into the stationary phase. Measurement of kinetic parameters shows that the enzyme has a high affinity for fluoroacetaldehyde and glyc
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SANADA, MINORU, TETSUJI MIYANO, and SHUICHI IWADARE. ".BETA.-Ethynylserine, an antimetabolite of L-threonine, from Streptomyces cattleya." Journal of Antibiotics 39, no. 2 (1986): 304–5. http://dx.doi.org/10.7164/antibiotics.39.304.

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Williamson, J. M., E. Inamine, K. E. Wilson, A. W. Douglas, J. M. Liesch, and G. Albers-Schönberg. "Biosynthesis of the beta-lactam antibiotic, thienamycin, by Streptomyces cattleya." Journal of Biological Chemistry 260, no. 8 (1985): 4637–47. http://dx.doi.org/10.1016/s0021-9258(18)89118-9.

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PARESS, P. S., and S. L. STREICHER. "Glutamine Synthetase of Streptomyces cattleya: Purification and Regulation of Synthesis." Microbiology 131, no. 8 (1985): 1903–10. http://dx.doi.org/10.1099/00221287-131-8-1903.

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Houck, David R., and Edward Inamine. "Oxalic acid biosynthesis and oxalacetate acetylhydrolase activity in Streptomyces cattleya." Archives of Biochemistry and Biophysics 259, no. 1 (1987): 58–65. http://dx.doi.org/10.1016/0003-9861(87)90470-x.

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Dissertations / Theses on the topic "Streptomyces cattleya"

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Coyne, Vernon Errol. "Genetic studies of Streptomyces cattleya and Streptomyces olivaceus." Doctoral thesis, University of Cape Town, 1985. http://hdl.handle.net/11427/17599.

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Bibliography: pages 243-259.<br>Actinophage VCll is able to virulently infect 11 of the 20 Streptomyces strains tested. Examination of VCll infection of Streptomyces cattleya, Streptomyces olivaceus and Streptomyces lividans TC10 indicated the absence of restriction-modification systems which affect VCll infectivity of these Streptomyces strains.
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Moss, Steven J. "Fluorometabolite biosynthesis in Streptomyces cattleya." Thesis, Durham University, 1999. http://etheses.dur.ac.uk/4603/.

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Nature has evolved the ability to form a C-F bond, as exemplified by the bacterium Streptomyces cattleya, which elaborates fluoroacetate (FAc) and 4-fluorothreomne (4- FT). The mechanism of this bond formation are unknown. This thesis probes the biosynthesis of fluoroacetate and 4-fiuorothreonine and in doing so explores the C-F bond forming process. Feeding stable isotope enriched primary metabolites to S. cattleya, followed by (^19)F NMR and GCMS analysis of the resultant fluorometabolites, highlights the role of the glycolytic pathway in delivering a substrate for fluorination. 3-Fluoro-l-
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Amin, Muhammad Ruhul. "Biosynthesis of fluoroacetate and 4-fluorothreonine in Streptomyces cattleya." Thesis, Durham University, 1996. http://etheses.dur.ac.uk/5428/.

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This thesis describes results on the biosynthesis of fluoroacetate and 4-fluorothreonine by the bacterium Streptomyces cattleya. Exploratory (^14)C-radiolabelling experiments, designed to determine the relative incorporation of a range of metabolites into fluoroacetate, demonstrated that substrates such as glucose, glycine and serine were efficient precursors. [2-(^13)C]-Glycolate, [l,2-(^13)C(_2)]-glycolate, [2,2-(^2)H(_2)]-glycolate, DL-[3,4,4,4-(^2)H(_4)]-threonine, DL-[4,4,4-(^2)H(_3)]-threonine, [3,3,3-(^2)H(_3)]-alanine, [3-(^2)H]-fluoropyruvate and [3-(^2)H]-3-fluorolactate were synthes
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McGlinchey, Ryan. "Intermediates and enzymes involved in fluorometabolite biosynthesis in Streptomyces cattleya." Thesis, University of St Andrews, 2006. http://hdl.handle.net/10023/11000.

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Enzymatic halogenation occurs during the biosynthesis of more than 4,000 natural products. The presence of fluorinated natural products is much less common, with only 13 reported to date. The bacterium Streptomyces cattleya is known to biosynthesise two fluorinated secondary metabolites, fluoroacetate and 4-fluorothreonine. The precursor to these secondary metabolites is known to be fluoroacetaldehyde. It had previously been shown that a fluorination enzyme mediates a reaction between S-adenosyl-L-methionine (SAM) and F to generate 5'-fluoro-5'-deoxyadenosine (5'-FDA). This is the first commit
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Reid, Karen A. "Biochemical studies of fluoroacetate and 4-fluorothreonine biosynthesis in Streptomyces cattleya." Thesis, Queen's University Belfast, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241432.

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Onega, Mayca. "Studies and application of the enzymes of fluorometabolite biosynthesis in Streptomyces cattleya." Thesis, University of St Andrews, 2009. http://hdl.handle.net/10023/991.

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This thesis focuses on studies investigating the structure of intermediates involved in fluorometabolite biosynthesis, and the potential applications of the fluorinase enzyme in positron emission tomography (PET). Chapter 1 introduces the rare natural occurrence of fluorinated compounds. The bacterium Streptomyces cattleya is known to biosynthesise two fluorinated secondary metabolites: the toxin fluoroacetate (FAc) and the antibiotic 4-fluorothreonine (4-FT). The enzymes and intermediates identified on this fluorometabolite biosynthetic pathway in S. cattleya, prior to this research, are disc
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Chan, K. K. Jason. "Identification and enzyme studies of rare amino acid biosynthesis from Streptomyces cattleya." Thesis, University of St Andrews, 2013. http://hdl.handle.net/10023/4478.

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This thesis is focussed on the biosynthesis of three toxins: fluoroacetate, 4-fluoro-L-theronine and β-ethynyl-L-serine which are biosynthesised by the soil bacteria Streptomyces cattleya. The two fluorinated metabolites originate from a common biosynthetic pathway and the thesis describes studies carried out on an aldose-ketose isomerase enzyme of the pathway. The biosynthetic origin of β-ethynyl-L-serine is not known. A total synthesis of this acetylenic amino acid is descibed along with the development of a new analytical method for identifying the metabolite and for future isotope-labellin
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Cross, Stuart. "In vitro studies of the enzymes involved in fluorometabolite biosynthesis in Streptomyces cattleya /." St Andrews, 2009. http://hdl.handle.net/10023/720.

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Cross, Stuart M. "In vitro studies of the enzymes involved in fluorometabolite biosynthesis in Streptomyces cattleya." Thesis, University of St Andrews, 2009. http://hdl.handle.net/10023/720.

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Enzymatic fluorination of natural products is extremely rare. Of the 4000 halogenated natural products identified, only 13 possess a fluorine atom. The C-F bond forming enzyme from the soil bacterium, Streptomyces cattleya, remains the only native enzyme to be identified that is capable of such biochemistry. It generates 5’-fluoro-5-deoxyadenosine (5‘-FDA) from S-adenosyl-L-methionine (SAM) and F-. The “fluorinase” is the first committed step toward the biosynthesis of the two fluorometabolites, 4-fluorothreonine and fluoroacetate, via the common intermediate, fluoroacetaldehyde (FAld). The en
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Goss, Rebecca Jane Miriam. "Biosynthetic studies on fluoroacetate and longianone." Thesis, Durham University, 2000. http://etheses.dur.ac.uk/4546/.

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This thesis explores the biosynthesis of two secondary metabolites, fluoroacetate and longianone, and involves the synthesis and feeding of deuterated putative intermediates. The bacterium Streptomyces cattleya produces fluoroacetate and 4- fluorothreonine; the mechanism by which C-F bond formation occurs is unknown. The stereochemistry of the fluorination event was investigated by feeding [2,2,3,3-(^-2)H(_4)]-succinate and (2R)-[l-(^2)H(_2)]- and (2S)-[l-(^2)H(_2)]-glycerols. The chirality of the resultant [2-(^2)H]-fluoroacetate was determined by chiral liquid crystal (^2)H-NMR and the fluor
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Book chapters on the topic "Streptomyces cattleya"

1

Reid, Karen A., Roy D. Bowden, and David B. Harper. "Biosynthesis of fluoroacetate and 4-fluorothreonine by Streptomyces cattleya." In Environment & Chemistry. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0061-8_25.

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Deng, Hai, Fang‐Lu Huang, James H. Naismith, David O'Hagan, Jonathan B. Spencer, and Xiaofeng Zhu. "Biological Fluorination in Streptomyces cattleya." In Fluorine and Health. Elsevier, 2008. http://dx.doi.org/10.1016/b978-0-444-53086-8.00018-7.

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Journal articles
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