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Items: 1 to 20 of 170

1.

A polyketide synthase of Plumbago indica that catalyzes the formation of hexaketide pyrones.

Springob K, Samappito S, Jindaprasert A, Schmidt J, Page JE, De-Eknamkul W, Kutchan TM.

FEBS J. 2007 Jan;274(2):406-17.

2.

Pyrone polyketides synthesized by a type III polyketide synthase from Drosophyllum lusitanicum.

Jindaprasert A, Springob K, Schmidt J, De-Eknamkul W, Kutchan TM.

Phytochemistry. 2008 Dec;69(18):3043-53. doi: 10.1016/j.phytochem.2008.03.013.

PMID:
18466932
3.

Novel type III polyketide synthases from Aloe arborescens.

Mizuuchi Y, Shi SP, Wanibuchi K, Kojima A, Morita H, Noguchi H, Abe I.

FEBS J. 2009 Apr;276(8):2391-401.

PMID:
19348024
4.

The first plant type III polyketide synthase that catalyzes formation of aromatic heptaketide.

Abe I, Utsumi Y, Oguro S, Noguchi H.

FEBS Lett. 2004 Mar 26;562(1-3):171-6.

5.

A novel quinone-forming monooxygenase family involved in modification of aromatic polyketides.

Funa N, Funabashi M, Yoshimura E, Horinouchi S.

J Biol Chem. 2005 Apr 15;280(15):14514-23.

6.

Engineered biosynthesis of plant polyketides: chain length control in an octaketide-producing plant type III polyketide synthase.

Abe I, Oguro S, Utsumi Y, Sano Y, Noguchi H.

J Am Chem Soc. 2005 Sep 14;127(36):12709-16.

PMID:
16144421
7.

Structure-based engineering of a plant type III polyketide synthase: formation of an unnatural nonaketide naphthopyrone.

Abe I, Morita H, Oguro S, Noma H, Wanibuchi K, Kawahara N, Goda Y, Noguchi H, Kohno T.

J Am Chem Soc. 2007 May 9;129(18):5976-80.

PMID:
17439126
8.

Crystal structure of a bacterial type III polyketide synthase and enzymatic control of reactive polyketide intermediates.

Austin MB, Izumikawa M, Bowman ME, Udwary DW, Ferrer JL, Moore BS, Noel JP.

J Biol Chem. 2004 Oct 22;279(43):45162-74.

9.

Aromatic and pyrone polyketides synthesized by a stilbene synthase from Rheum tataricum.

Samappito S, Page JE, Schmidt J, De-Eknamkul W, Kutchan TM.

Phytochemistry. 2003 Feb;62(3):313-23.

PMID:
12620343
10.

Aspergillus oryzae CsyB catalyzes the condensation of two β-ketoacyl-CoAs to form 3-acetyl-4-hydroxy-6-alkyl-α-pyrone.

Hashimoto M, Koen T, Takahashi H, Suda C, Kitamoto K, Fujii I.

J Biol Chem. 2014 Jul 18;289(29):19976-84. doi: 10.1074/jbc.M114.569095.

11.

A type III polyketide synthase from Wachendorfia thyrsiflora and its role in diarylheptanoid and phenylphenalenone biosynthesis.

Brand S, Hölscher D, Schierhorn A, Svatos A, Schröder J, Schneider B.

Planta. 2006 Jul;224(2):413-28.

PMID:
16496097
12.

A type III polyketide synthase from Rhizobium etli condenses malonyl CoAs to a heptaketide pyrone with unusually high catalytic efficiency.

Jeya M, Kim TS, Kumar Tiwari M, Li J, Zhao H, Lee JK.

Mol Biosyst. 2012 Oct 30;8(12):3103-6. doi: 10.1039/c2mb25347j.

PMID:
23059854
13.

Structure function analysis of novel type III polyketide synthases from Arabidopsis thaliana.

Mizuuchi Y, Shimokawa Y, Wanibuchi K, Noguchi H, Abe I.

Biol Pharm Bull. 2008 Dec;31(12):2205-10.

14.

Polyketide synthesis in tobacco plants transformed with a Plumbago zeylanica type III hexaketide synthase.

Jadhav S, Phapale P, Thulasiram HV, Bhargava S.

Phytochemistry. 2014 Feb;98:92-100. doi: 10.1016/j.phytochem.2013.11.017.

PMID:
24355695
15.

Molecular characterization of root-specific chalcone synthases from Cassia alata.

Samappito S, Page J, Schmidt J, De-Eknamkul W, Kutchan TM.

Planta. 2002 Nov;216(1):64-71.

PMID:
12430015
16.
17.

Structural control of polyketide formation in plant-specific polyketide synthases.

Jez JM, Austin MB, Ferrer J, Bowman ME, Schröder J, Noel JP.

Chem Biol. 2000 Dec;7(12):919-30.

18.

Dissection of malonyl-coenzyme A decarboxylation from polyketide formation in the reaction mechanism of a plant polyketide synthase.

Jez JM, Ferrer JL, Bowman ME, Dixon RA, Noel JP.

Biochemistry. 2000 Feb 8;39(5):890-902.

PMID:
10653632
19.
20.

Octaketide-producing type III polyketide synthase from Hypericum perforatum is expressed in dark glands accumulating hypericins.

Karppinen K, Hokkanen J, Mattila S, Neubauer P, Hohtola A.

FEBS J. 2008 Sep;275(17):4329-42. doi: 10.1111/j.1742-4658.2008.06576.x.

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