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| Names | |
|---|---|
|
IUPAC name
2-methoxy-3,5-dimethyl-6-[(2R,4Z)-4-[(E)-2-methyl-3-(4-nitrophenyl)prop-2-enylidene]oxolan-2-yl]pyran-4-one
[1]
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ChEBI | |
| ChemSpider | |
| KEGG | |
PubChem
CID
|
|
| UNII | |
| |
| |
| Properties | |
| C22H23NO6 | |
| Molar mass | 397.427 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Aureothin is a natural product of a cytotoxic shikimate- polyketide antibiotic with the molecular formula C22H23NO6. [2] [3] [1] Aureothin is produced by the bacterium Streptomyces thioluteus [3] [4] that illustrates antitumor, antifungal, and insecticidal activities and the new aureothin derivatives can be antifungal and antiproliferative. [2] In addition, aureothin, a nitro compound from Streptomyces thioluteus, was indicated to have pesticidal activity against the bean weevil [5] by interfering with mitochondrial respiratory complex II. [6]
Biosynthesis
Regarding the biosynthesis of aureothin, the biosynthetic pathway would be begun with chorismic acid. P-nitrobenzoate is derived from p-aminobenzoate by an N-oxygenase, which is encoded by aurF. [7] The aurF is one of the aureothin biosynthetic enzymes and it is referred to as a nonheme diiron oxygenase that is responsible for converting p-aminobenzoate to p-nitrobenzoate. [8] Moreover, the aurF catalyzes a reaction of a complete six-electron oxidation utilizing two equivalents of dioxygen and two exogenous electrons in order to convert p-aminobenzoate to p-nitrobenzoate. [8] Then, three type I Polyketide Synthases (PKSs), which is encoded by aurA, aurB, and aurC, generates the a polyketide chain using p-nitrobenzoate as a starter unit [9] for the biosynthesis of aureothin. At this point, the repetition that one molecule catalyzes two successive cycles of chain extension would occur in the reaction of the type I Polyketide Synthase (PKS). [10] In particular, the two consecutive cycles containing four times of methylmalonyl-CoA and one time of malonyl-CoA occur during the type I Polyketide Synthase (PKS). After O-methylation is activated by a methyltransferase, which is encoded by aurI, the tetrahydrofuran ring formation is produced by a monooxygenase that is encoded by aurH. Therefore, the final product, aureothin, is produced as a result of the monooxygenase encoded by aurH. [11]
References
- ^ a b "Aureothin". Pubchem.
- ^ a b Issues in Chemistry and General Chemical Research (2011 ed.). ScholarlyEditions. 9 January 2012. p. 442. ISBN 978-1-4649-6334-6.
- ^ a b He, Jing; Hertweck, Christian (1 March 2004). "Biosynthetic Origin of the Rare Nitroaryl Moiety of the Polyketide Antibiotic Aureothin: Involvement of an Unprecedented N-Oxygenase". Journal of the American Chemical Society. 126 (12): 3694–3695. doi: 10.1021/ja039328t. PMID 15038705.
- ^ Hirata, Yoshimasa; Nakata, Hisao; Yamada, Kiyoyuki; Okuhara, Kunio; Naito, Takayuki (January 1961). "The structure of aureothin, a nitro compound obtained from Streptomyces thioluteus". Tetrahedron. 14 (3–4): 252–274. doi: 10.1016/S0040-4020(01)92175-1.
- ^ Oishi, H.; Hosokawa, T.; Okutomi, T.; Suzuki, K. (1969). "Pesticidal Activity of Aureothin". Agricultural and Biological Chemistry. 33 (12): 1790–1791. doi: 10.1080/00021369.1969.10859541.
- ^ Friedrich, T; Van Heek, P; Leif, H; Ohnishi, T; Forche, E; Kunze, B; Jansen, R; Trowitzsch-Kienast, W; Hofle, G; Reichenhach, H (1994). "Two binding sites of inhibitors in NADH: ubiquinone oxidoreductase (complex I). Relationship of one site with the ubiquinone-binding site of bacterial glucose:ubiquinone oxidoreductase". Eur. J. Biochem. 219 (1): 691–698. doi: 10.1111/j.1432-1033.1994.tb19985.x. PMID 8307034.
- ^ He, Jing; Hertweck, Christian (2004). "Biosynthetic Origin of the Rare Nitroaryl Moiety of the Polyketide Antibiotic Aureothin: Involvement of an Unprecedented N-Oxygenase". J. Am. Chem. Soc. 126 (12): 3694–3695. doi: 10.1021/ja039328t. PMID 15038705.
- ^ a b Tsunematsu, Yuta; Hirayama, Yuichiro; Masuya, Takahiro; Watanabe, Kenji (2020). "Oxidative Modification Enzymes in Polyketide Biosynthetic Pathways". Comprehensive Natural Products III (Third Edition). 1: 479–505. doi: 10.1016/B978-0-12-409547-2.14637-2. ISBN 9780081026915. S2CID 201202729.
- ^ He, Jing; Hertweck, Christian (2005). "Functional Analysis of the Aureothin Iterative Type I Polyketide Synthase". ChemBioChem. 6 (5): 908–912. doi: 10.1002/cbic.200400333. PMID 15812854. S2CID 27585538.
- ^ He, Jing; Hertweck, Christian (2004). "Biosynthetic Origin of the Rare Nitroaryl Moiety of the Polyketide Antibiotic Aureothin: Involvement of an Unprecedented N-Oxygenase". J. Am. Chem. Soc. 126 (12): 3694–3695. doi: 10.1021/ja039328t. PMID 15038705.
- ^ Sugimoto, Yuki; Ishida, Keishi; Traitcheva, Nelly; Busch, Benjamin; Dahse, Hans-Martin; Hertweck, Christian. "Freedom and Constraint in Engineered Noncolinear Polyketide Assembly Lines". ChemBioChem. 10 (7): 1225–1232.
- ^ Sakuda, Shohei; Kimura, Makoto (2010). "Toxins of Microorganisms". Comprehensive Natural Products II. 4: 411–455. doi: 10.1016/B978-008045382-8.00102-7. ISBN 9780080453828.
Further reading
- Natural Product Biosynthesis by Microorganisms and Plants Part C. Academic Press. 31 December 2012. p. 216. ISBN 978-0-12-404617-7.
- Strategies and Tactics in Organic Synthesis. Elsevier. 4 October 2016. p. 120. ISBN 978-0-08-100762-4.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
|
| |
| Names | |
|---|---|
|
IUPAC name
2-methoxy-3,5-dimethyl-6-[(2R,4Z)-4-[(E)-2-methyl-3-(4-nitrophenyl)prop-2-enylidene]oxolan-2-yl]pyran-4-one
[1]
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ChEBI | |
| ChemSpider | |
| KEGG | |
PubChem
CID
|
|
| UNII | |
| |
| |
| Properties | |
| C22H23NO6 | |
| Molar mass | 397.427 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Aureothin is a natural product of a cytotoxic shikimate- polyketide antibiotic with the molecular formula C22H23NO6. [2] [3] [1] Aureothin is produced by the bacterium Streptomyces thioluteus [3] [4] that illustrates antitumor, antifungal, and insecticidal activities and the new aureothin derivatives can be antifungal and antiproliferative. [2] In addition, aureothin, a nitro compound from Streptomyces thioluteus, was indicated to have pesticidal activity against the bean weevil [5] by interfering with mitochondrial respiratory complex II. [6]
Biosynthesis
Regarding the biosynthesis of aureothin, the biosynthetic pathway would be begun with chorismic acid. P-nitrobenzoate is derived from p-aminobenzoate by an N-oxygenase, which is encoded by aurF. [7] The aurF is one of the aureothin biosynthetic enzymes and it is referred to as a nonheme diiron oxygenase that is responsible for converting p-aminobenzoate to p-nitrobenzoate. [8] Moreover, the aurF catalyzes a reaction of a complete six-electron oxidation utilizing two equivalents of dioxygen and two exogenous electrons in order to convert p-aminobenzoate to p-nitrobenzoate. [8] Then, three type I Polyketide Synthases (PKSs), which is encoded by aurA, aurB, and aurC, generates the a polyketide chain using p-nitrobenzoate as a starter unit [9] for the biosynthesis of aureothin. At this point, the repetition that one molecule catalyzes two successive cycles of chain extension would occur in the reaction of the type I Polyketide Synthase (PKS). [10] In particular, the two consecutive cycles containing four times of methylmalonyl-CoA and one time of malonyl-CoA occur during the type I Polyketide Synthase (PKS). After O-methylation is activated by a methyltransferase, which is encoded by aurI, the tetrahydrofuran ring formation is produced by a monooxygenase that is encoded by aurH. Therefore, the final product, aureothin, is produced as a result of the monooxygenase encoded by aurH. [11]
References
- ^ a b "Aureothin". Pubchem.
- ^ a b Issues in Chemistry and General Chemical Research (2011 ed.). ScholarlyEditions. 9 January 2012. p. 442. ISBN 978-1-4649-6334-6.
- ^ a b He, Jing; Hertweck, Christian (1 March 2004). "Biosynthetic Origin of the Rare Nitroaryl Moiety of the Polyketide Antibiotic Aureothin: Involvement of an Unprecedented N-Oxygenase". Journal of the American Chemical Society. 126 (12): 3694–3695. doi: 10.1021/ja039328t. PMID 15038705.
- ^ Hirata, Yoshimasa; Nakata, Hisao; Yamada, Kiyoyuki; Okuhara, Kunio; Naito, Takayuki (January 1961). "The structure of aureothin, a nitro compound obtained from Streptomyces thioluteus". Tetrahedron. 14 (3–4): 252–274. doi: 10.1016/S0040-4020(01)92175-1.
- ^ Oishi, H.; Hosokawa, T.; Okutomi, T.; Suzuki, K. (1969). "Pesticidal Activity of Aureothin". Agricultural and Biological Chemistry. 33 (12): 1790–1791. doi: 10.1080/00021369.1969.10859541.
- ^ Friedrich, T; Van Heek, P; Leif, H; Ohnishi, T; Forche, E; Kunze, B; Jansen, R; Trowitzsch-Kienast, W; Hofle, G; Reichenhach, H (1994). "Two binding sites of inhibitors in NADH: ubiquinone oxidoreductase (complex I). Relationship of one site with the ubiquinone-binding site of bacterial glucose:ubiquinone oxidoreductase". Eur. J. Biochem. 219 (1): 691–698. doi: 10.1111/j.1432-1033.1994.tb19985.x. PMID 8307034.
- ^ He, Jing; Hertweck, Christian (2004). "Biosynthetic Origin of the Rare Nitroaryl Moiety of the Polyketide Antibiotic Aureothin: Involvement of an Unprecedented N-Oxygenase". J. Am. Chem. Soc. 126 (12): 3694–3695. doi: 10.1021/ja039328t. PMID 15038705.
- ^ a b Tsunematsu, Yuta; Hirayama, Yuichiro; Masuya, Takahiro; Watanabe, Kenji (2020). "Oxidative Modification Enzymes in Polyketide Biosynthetic Pathways". Comprehensive Natural Products III (Third Edition). 1: 479–505. doi: 10.1016/B978-0-12-409547-2.14637-2. ISBN 9780081026915. S2CID 201202729.
- ^ He, Jing; Hertweck, Christian (2005). "Functional Analysis of the Aureothin Iterative Type I Polyketide Synthase". ChemBioChem. 6 (5): 908–912. doi: 10.1002/cbic.200400333. PMID 15812854. S2CID 27585538.
- ^ He, Jing; Hertweck, Christian (2004). "Biosynthetic Origin of the Rare Nitroaryl Moiety of the Polyketide Antibiotic Aureothin: Involvement of an Unprecedented N-Oxygenase". J. Am. Chem. Soc. 126 (12): 3694–3695. doi: 10.1021/ja039328t. PMID 15038705.
- ^ Sugimoto, Yuki; Ishida, Keishi; Traitcheva, Nelly; Busch, Benjamin; Dahse, Hans-Martin; Hertweck, Christian. "Freedom and Constraint in Engineered Noncolinear Polyketide Assembly Lines". ChemBioChem. 10 (7): 1225–1232.
- ^ Sakuda, Shohei; Kimura, Makoto (2010). "Toxins of Microorganisms". Comprehensive Natural Products II. 4: 411–455. doi: 10.1016/B978-008045382-8.00102-7. ISBN 9780080453828.
Further reading
- Natural Product Biosynthesis by Microorganisms and Plants Part C. Academic Press. 31 December 2012. p. 216. ISBN 978-0-12-404617-7.
- Strategies and Tactics in Organic Synthesis. Elsevier. 4 October 2016. p. 120. ISBN 978-0-08-100762-4.
|
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |