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Volumn 141, Issue 50, 2019, Pages 19538-19541

Fungal highly reducing polyketide synthases biosynthesize salicylaldehydes that are precursors to epoxycyclohexenol natural products

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMISTRY; BIOSYNTHESIS; CONDENSATION REACTIONS; DEHYDROGENATION; ENZYMES; GENES;

EID: 85076251225     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.9b09669     Document Type: Article
Times cited : (49)

References (24)
  • 1
    • 34250790717 scopus 로고    scopus 로고
    • Polyketides, proteins and genes in fungi: Programmed nano-machines begin to reveal their secrets
    • Cox, R. J. Polyketides, proteins and genes in fungi: programmed nano-machines begin to reveal their secrets. Org. Biomol. Chem. 2007, 5, 2010–2026.
    • (2007) Org. Biomol. Chem. , vol.5 , pp. 2010-2026
    • Cox, R.J.1
  • 2
    • 84869169169 scopus 로고    scopus 로고
    • Navigating the fungal polyketide chemical space: From genes to molecules
    • Chooi, Y. H.; Tang, Y. Navigating the fungal polyketide chemical space: from genes to molecules. J. Org. Chem. 2012, 77, 9933–9953.
    • (2012) J. Org. Chem. , vol.77 , pp. 9933-9953
    • Chooi, Y.H.1    Tang, Y.2
  • 3
    • 0033591447 scopus 로고    scopus 로고
    • Modulation of polyketide synthase activity by accessory proteins during lovastatin biosynthesis
    • Kennedy, J.; Auclair, K.; Kendrew, S. G.; Park, C.; Vederas, J. C.; Hutchinson, C. R. Modulation of polyketide synthase activity by accessory proteins during lovastatin biosynthesis. Science 1999, 284, 1368–1372.
    • (1999) Science , vol.284 , pp. 1368-1372
    • Kennedy, J.1    Auclair, K.2    Kendrew, S.G.3    Park, C.4    Vederas, J.C.5    Hutchinson, C.R.6
  • 4
    • 72149134196 scopus 로고    scopus 로고
    • Genes, gene clusters, and biosynthesis of trichothecenes and fumonisins in Fusarium
    • Alexander, N. J.; Proctor, R. H.; McCormick, S. P. Genes, gene clusters, and biosynthesis of trichothecenes and fumonisins in Fusarium. Toxin Rev. 2009, 28, 198–215.
    • (2009) Toxin Rev , vol.28 , pp. 198-215
    • Alexander, N.J.1    Proctor, R.H.2    McCormick, S.P.3
  • 5
    • 77953035258 scopus 로고    scopus 로고
    • Cyclization of aromatic polyketides from bacteria and fungi
    • Zhou, H.; Li, Y.; Tang, Y. Cyclization of aromatic polyketides from bacteria and fungi. Nat. Prod. Rep. 2010, 27, 839–868.
    • (2010) Nat. Prod. Rep. , vol.27 , pp. 839-868
    • Zhou, H.1    Li, Y.2    Tang, Y.3
  • 6
    • 85065032822 scopus 로고    scopus 로고
    • Genome mining reveals Neurospora crassa can produce the salicylaldehyde sordarial
    • Zhao, Z.; Ying, Y.; Hung, Y. S.; Tang, Y. Genome mining reveals Neurospora crassa can produce the salicylaldehyde sordarial. J. Nat. Prod. 2019, 82, 1029–1033.
    • (2019) J. Nat. Prod. , vol.82 , pp. 1029-1033
    • Zhao, Z.1    Ying, Y.2    Hung, Y.S.3    Tang, Y.4
  • 9
    • 0141571260 scopus 로고    scopus 로고
    • A cyclic carbonate and related polyketides from a marine-derived fungus of the genus Phoma
    • a
    • (a) Liu, Z.; Jensen, P. R.; Fenical, W. A cyclic carbonate and related polyketides from a marine-derived fungus of the genus Phoma. Phytochemistry 2003, 64, 571–574.
    • (2003) Phytochemistry , vol.64 , pp. 571-574
    • Liu, Z.1    Jensen, P.R.2    Fenical, W.3
  • 10
    • 3242728831 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (+)-eupenoxide and (+)-phomoxide: Revision of structures and assignment of absolute configuration
    • Mehta, G.; Roy, S. Enantioselective total synthesis of (+)-eupenoxide and (+)-phomoxide: revision of structures and assignment of absolute configuration. Org. Lett. 2004, 6, 2389–2392.
    • (2004) Org. Lett. , vol.6 , pp. 2389-2392
    • Mehta, G.1    Roy, S.2
  • 11
    • 47049089764 scopus 로고    scopus 로고
    • On the stereostructures of (+)-eupenoxide and (–)-3′,4’ dihydrophomoxide: A caveat on the spectral comparisons of oxygenated cyclohexenoids
    • Mehta, G.; Roy, S.; Davis, R. A. On the stereostructures of (+)-eupenoxide and (–)-3′,4’ dihydrophomoxide: a caveat on the spectral comparisons of oxygenated cyclohexenoids. Tetrahedron Lett. 2008, 49, 5162–5164.
    • (2008) Tetrahedron Lett , vol.49 , pp. 5162-5164
    • Mehta, G.1    Roy, S.2    Davis, R.A.3
  • 12
    • 85025127755 scopus 로고    scopus 로고
    • Selected mutations revealed intermediates and key precursors in the biosynthesis of polyketide-terpenoid hybrid sesquiterpenyl epoxy-cyclohexenoids
    • a
    • (a) Teng, L. L.; Song, T. Y.; Xu, Z. F.; Liu, X.; Dai, R.; Chen, Y. H.; Li, S. H.; Zhang, K. Q.; Niu, X. M. Selected mutations revealed intermediates and key precursors in the biosynthesis of polyketide-terpenoid hybrid sesquiterpenyl epoxy-cyclohexenoids. Org. Lett. 2017, 19, 3923–3926.
    • (2017) Org. Lett. , vol.19 , pp. 3923-3926
    • Teng, L.L.1    Song, T.Y.2    Xu, Z.F.3    Liu, X.4    Dai, R.5    Chen, Y.H.6    Li, S.H.7    Zhang, K.Q.8    Niu, X.M.9
  • 15
    • 45249117900 scopus 로고    scopus 로고
    • Aurocitrin and related polyketide metabolites from the wood-decay fungus Hypocrea sp. BCC 14122
    • Berkaew, P.; Soonthornchareonnon, N.; Salasawadee, K.; Chanthaket, R.; Isaka, M. Aurocitrin and related polyketide metabolites from the wood-decay fungus Hypocrea sp. BCC 14122. J. Nat. Prod. 2008, 71, 902–904.
    • (2008) J. Nat. Prod. , vol.71 , pp. 902-904
    • Berkaew, P.1    Soonthornchareonnon, N.2    Salasawadee, K.3    Chanthaket, R.4    Isaka, M.5
  • 16
    • 0000660074 scopus 로고
    • Ring-chain tautomerism of hydroxy aldehydes
    • a
    • (a) Hurd, C. D.; Saunders, W. H., Jr. Ring-chain tautomerism of hydroxy aldehydes. J. Am. Chem. Soc. 1952, 74, 5324–5329.
    • (1952) J. Am. Chem. Soc. , vol.74 , pp. 5324-5329
    • Hurd, C.D.1    Saunders, W.H.2
  • 17
    • 33947481934 scopus 로고
    • Ring-chain tautomerism
    • Jones, P. R. Ring-chain tautomerism. Chem. Rev. 1963, 63, 461–487.
    • (1963) Chem. Rev. , vol.63 , pp. 461-487
    • Jones, P.R.1
  • 18
    • 84938858793 scopus 로고    scopus 로고
    • Determination of the in vivo NAD:NADH ratio in Saccharomyces cerevisiae under anaerobic conditions, using alcohol dehydrogenase as sensor reaction
    • Bekers, K. M.; Heijnen, J. J.; van Gulik, W. M. Determination of the in vivo NAD:NADH ratio in Saccharomyces cerevisiae under anaerobic conditions, using alcohol dehydrogenase as sensor reaction. Yeast 2015, 32, 541–557.
    • (2015) Yeast , vol.32 , pp. 541-557
    • Bekers, K.M.1    Heijnen, J.J.2    Van Gulik, W.M.3
  • 19
    • 0034958892 scopus 로고    scopus 로고
    • Purification and characterisation of the water forming NADH-oxidase from Lactococcuslactis
    • a
    • (a) Lopez de Felipe, F.; Hugenholtz, J. Purification and characterisation of the water forming NADH-oxidase from Lactococcuslactis. Int. Dairy J. 2001, 11, 37–44.
    • (2001) Int. Dairy J. , vol.11 , pp. 37-44
    • Lopez De Felipe, F.1    Hugenholtz, J.2
  • 20
    • 79958041001 scopus 로고    scopus 로고
    • Identification of a conserved sequence in flavoproteins essential for the correct conformation and activity of the NADH oxidase NoxE of Lactococcuslactis
    • Tachon, S.; Chambellon, E.; Yvon, M. Identification of a conserved sequence in flavoproteins essential for the correct conformation and activity of the NADH oxidase NoxE of Lactococcuslactis. J. Bacteriol. 2011, 193, 3000–3008.
    • (2011) J. Bacteriol. , vol.193 , pp. 3000-3008
    • Tachon, S.1    Chambellon, E.2    Yvon, M.3
  • 22
    • 85056115136 scopus 로고    scopus 로고
    • Resorcylic acid lactones (RALs) and their structural congeners: Recent advances in their biosynthesis, chemical synthesis and biology
    • Jana, N.; Nanda, S. Resorcylic acid lactones (RALs) and their structural congeners: recent advances in their biosynthesis, chemical synthesis and biology. New J. Chem. 2018, 42, 17803–17873.
    • (2018) New J. Chem. , vol.42 , pp. 17803-17873
    • Jana, N.1    Nanda, S.2
  • 23
    • 84953432269 scopus 로고    scopus 로고
    • Discovery of unclustered fungal indole diterpene biosynthetic pathways through combinatorial pathway reassembly in engineered yeast
    • Tang, M. C.; Lin, H. C.; Li, D. H.; Zou, Y.; Li, J.; Xu, W.; Cacho, R. A.; Hillenmeyer, M. E.; Garg, N. K.; Tang, Y. Discovery of unclustered fungal indole diterpene biosynthetic pathways through combinatorial pathway reassembly in engineered yeast. J. Am. Chem. Soc. 2015, 137, 13724–13727.
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 13724-13727
    • Tang, M.C.1    Lin, H.C.2    Li, D.H.3    Zou, Y.4    Li, J.5    Xu, W.6    Cacho, R.A.7    Hillenmeyer, M.E.8    Garg, N.K.9    Tang, Y.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.