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Generation of Complexity in Fungal Terpene Biosynthesis: Discovery of a Multifunctional Cytochrome P450 in the Fumagillin Pathway

CITE Title : Generation of Complexity in Fungal Terpene Biosynthesis: Discovery of a Multifunctional Cytochrome P450 in the Fumagillin Pathway Personal Author(s) : Lin, Hsiao-Ching;Tsunematsu, Yuta;Dhingra, Sourabh;Xu, Wei;Fukutomi, Manami;Chooi, Yit-Heng;Cane, David E.;Calvo, Ana M.;Watanabe, Kenji;Tang, Yi; Published Date : Mar 11 2014 Source : J Am Chem Soc. 2014; 136(11):4426-4436. URL : https://stacks.cdc.gov/view/cdc/32204 Lin, Hsiao-Ching et al. (2014). Generation of Complexity in Fungal Terpene Biosynthesis: Discovery of a Multifunctional Cytochrome P450 in the Fumagillin Pathway. 136(11). Lin, Hsiao-Ching et al. "Generation of Complexity in Fungal Terpene Biosynthesis: Discovery of a Multifunctional Cytochrome P450 in the Fumagillin Pathway" 136, no. 11 (2014) Lin, Hsiao-Ching et al. "Generation of Complexity in Fungal Terpene Biosynthesis: Discovery of a Multifunctional Cytochrome P450 in the Fumagillin Pathway" vol. 136, no. 11, 2014 Export RIS Citation Information.

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Lin, Hsiao-Ching ;

Tsunematsu, Yuta

Mar 11 2014 | J Am Chem Soc. 2014; 136(11):4426-4436.

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Fumagillin (1), a meroterpenoid from Aspergillus fumigatus, is known for its antiangiogenic activity due to binding to human methionine aminopeptidase...
Identification and Characterization of the Echinocandin B Biosynthetic Gene Cluster from Emericella rugulosa NRRL 11440

CITE Title : Identification and Characterization of the Echinocandin B Biosynthetic Gene Cluster from Emericella rugulosa NRRL 11440 Personal Author(s) : Cacho, Ralph A.;Jiang, Wei;Chooi, Yit-Heng;Walsh, Christopher T.;Tang, Yi; Published Date : 10 10 2012;10-10-; Source : J Am Chem Soc. 134(40):16781-16790 URL : https://stacks.cdc.gov/view/cdc/33455 Cacho, Ralph A. et al. (2012). Identification and Characterization of the Echinocandin B Biosynthetic Gene Cluster from Emericella rugulosa NRRL 11440. 134(40). Cacho, Ralph A. et al. "Identification and Characterization of the Echinocandin B Biosynthetic Gene Cluster from Emericella rugulosa NRRL 11440" 134, no. 40 (2012) Cacho, Ralph A. et al. "Identification and Characterization of the Echinocandin B Biosynthetic Gene Cluster from Emericella rugulosa NRRL 11440" vol. 134, no. 40, 2012 Export RIS Citation Information.

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Cacho, Ralph A. ;

Jiang, Wei

10 10 2012 | J Am Chem Soc. 134(40):16781-16790

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Echinocandins are a family of fungal lipidated cyclic hexapeptide natural products. Due to their effectiveness as antifungal agents, three semisynthet...
Efficient Biosynthesis of Fungal Polyketides Containing the Dioxabicyclo-octane Ring System

CITE Title : Efficient Biosynthesis of Fungal Polyketides Containing the Dioxabicyclo-octane Ring System Personal Author(s) : Mao, Xu-Ming;Zhan, Zha-Jun;Grayson, Matthew N.;Tang, Man-Cheng;Xu, Wei;Li, Yong-Quan;Yin, Wen-Bing;Lin, Hsiao-Ching;Chooi, Yit-Heng;Houk, K. N.;Tang, Yi; Published Date : 9-23- Source : J Am Chem Soc. 137(37):11904-11907 URL : https://stacks.cdc.gov/view/cdc/39865 Mao, Xu-Ming et al. (2016). Efficient Biosynthesis of Fungal Polyketides Containing the Dioxabicyclo-octane Ring System. 137(37). Mao, Xu-Ming et al. "Efficient Biosynthesis of Fungal Polyketides Containing the Dioxabicyclo-octane Ring System" 137, no. 37 (2016) Mao, Xu-Ming et al. "Efficient Biosynthesis of Fungal Polyketides Containing the Dioxabicyclo-octane Ring System" vol. 137, no. 37, 2016 Export RIS Citation Information.

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Mao, Xu-Ming ;

Zhan, Zha-Jun

9-23- | J Am Chem Soc. 137(37):11904-11907

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Aurovertins are fungal polyketides that exhibit potent inhibition of adenosine triphosphate synthase. Aurovertins contain a 2,6-dioxabicyclo[3.2.1]oct...
Complexity generation in fungal polyketide biosynthesis: a spirocycle-forming P450 in the concise pathway to the antifungal drug griseofulvin

CITE Title : Complexity generation in fungal polyketide biosynthesis: a spirocycle-forming P450 in the concise pathway to the antifungal drug griseofulvin Personal Author(s) : Cacho, Ralph A.;Chooi, Yit-Heng;Zhou, Hui;Tang, Yi; Published Date : 10 18 2013;10-18-; Source : ACS Chem Biol. 8(10):2322-2330 URL : https://stacks.cdc.gov/view/cdc/29769 Cacho, Ralph A. et al. (2013). Complexity generation in fungal polyketide biosynthesis: a spirocycle-forming P450 in the concise pathway to the antifungal drug griseofulvin. 8(10). Cacho, Ralph A. et al. "Complexity generation in fungal polyketide biosynthesis: a spirocycle-forming P450 in the concise pathway to the antifungal drug griseofulvin" 8, no. 10 (2013) Cacho, Ralph A. et al. "Complexity generation in fungal polyketide biosynthesis: a spirocycle-forming P450 in the concise pathway to the antifungal drug griseofulvin" vol. 8, no. 10, 2013 Export RIS Citation Information.

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Cacho, Ralph A. ;

Chooi, Yit-Heng

10 18 2013 | ACS Chem Biol. 8(10):2322-2330

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Griseofulvin (1) is a spirocyclic fungal natural product used in treatment of fungal dermatophytes. Formation of the spirocycle, or the grisan scaffol...
The Fumagillin Biosynthetic Gene Cluster in Aspergillus fumigatus Encodes a Cryptic Terpene Cyclase Involved in the Formation of β-trans-Bergamotene

CITE Title : The Fumagillin Biosynthetic Gene Cluster in Aspergillus fumigatus Encodes a Cryptic Terpene Cyclase Involved in the Formation of β-trans-Bergamotene Personal Author(s) : Lin, Hsiao-Ching;Chooi, Yit-Heng;Dhingra, Sourabh;Xu, Wei;Calvo, Ana M.;Tang, Yi; Published Date : 3 27 2013;3-27-; Source : J Am Chem Soc. 135(12):4616-4619 URL : https://stacks.cdc.gov/view/cdc/29658 Lin, Hsiao-Ching et al. (2013). The Fumagillin Biosynthetic Gene Cluster in Aspergillus fumigatus Encodes a Cryptic Terpene Cyclase Involved in the Formation of β-trans-Bergamotene. 135(12). Lin, Hsiao-Ching et al. "The Fumagillin Biosynthetic Gene Cluster in Aspergillus fumigatus Encodes a Cryptic Terpene Cyclase Involved in the Formation of β-trans-Bergamotene" 135, no. 12 (2013) Lin, Hsiao-Ching et al. "The Fumagillin Biosynthetic Gene Cluster in Aspergillus fumigatus Encodes a Cryptic Terpene Cyclase Involved in the Formation of β-trans-Bergamotene" vol. 135, no. 12, 2013 Export RIS Citation Information.

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Lin, Hsiao-Ching ;

Chooi, Yit-Heng

3 27 2013 | J Am Chem Soc. 135(12):4616-4619

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Fumagillin 1 is a meroterpenoid from Aspergillus fumigatus that is known for its anti-angiogenic activity by binding to human methionine aminopeptidas...
Elucidation of the Concise Biosynthetic Pathway of the Communesin Indole Alkaloids

CITE Title : Elucidation of the Concise Biosynthetic Pathway of the Communesin Indole Alkaloids Personal Author(s) : Lin, Hsiao-Ching;Chiou, Grace;Chooi, Yit-Heng;McMahon, Travis C.;Xu, Wei;Garg, Neil K.;Tang, Yi; Published Date : 3 2 2015;3-2-; Source : Angew Chem Int Ed Engl. 54(10):3004-3007 URL : https://stacks.cdc.gov/view/cdc/30652 Lin, Hsiao-Ching et al. (2015). Elucidation of the Concise Biosynthetic Pathway of the Communesin Indole Alkaloids. 54(10). Lin, Hsiao-Ching et al. "Elucidation of the Concise Biosynthetic Pathway of the Communesin Indole Alkaloids" 54, no. 10 (2015) Lin, Hsiao-Ching et al. "Elucidation of the Concise Biosynthetic Pathway of the Communesin Indole Alkaloids" vol. 54, no. 10, 2015 Export RIS Citation Information.

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Lin, Hsiao-Ching ;

Chiou, Grace

3 2 2015 | Angew Chem Int Ed Engl. 54(10):3004-3007

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The communesins are a prominent class of indole alkaloids isolated from Penicillium species. Owing to their daunting structural framework and potentia...
Genome Mining of a Prenylated and Immunosuppressive Polyketide from Pathogenic Fungi

CITE Title : Genome Mining of a Prenylated and Immunosuppressive Polyketide from Pathogenic Fungi Personal Author(s) : Chooi, Yit-Heng;Fang, Jinxu;Liu, Hong;Filler, Scott G.;Wang, Pin;Tang, Yi; Published Date : 2 15 2013;2-15-; Source : Org Lett. 15(4):780-783 URL : https://stacks.cdc.gov/view/cdc/29623 Chooi, Yit-Heng et al. (2013). Genome Mining of a Prenylated and Immunosuppressive Polyketide from Pathogenic Fungi. 15(4). Chooi, Yit-Heng et al. "Genome Mining of a Prenylated and Immunosuppressive Polyketide from Pathogenic Fungi" 15, no. 4 (2013) Chooi, Yit-Heng et al. "Genome Mining of a Prenylated and Immunosuppressive Polyketide from Pathogenic Fungi" vol. 15, no. 4, 2013 Export RIS Citation Information.

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Chooi, Yit-Heng ;

Fang, Jinxu

2 15 2013 | Org Lett. 15(4):780-783

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Activation of the polycyclic polyketide prenyltransferase (pcPTase)-containing silent clusters in Aspergillus fumigatus and Neosartorya fischeri led t...
A Cytochrome P450 Serves as an Unexpected Terpene Cyclase during Fungal Meroterpenoid Biosynthesis

CITE Title : A Cytochrome P450 Serves as an Unexpected Terpene Cyclase during Fungal Meroterpenoid Biosynthesis Personal Author(s) : Chooi, Yit-Heng;Hong, Young J.;Cacho, Ralph A.;Tantillo, Dean J.;Tang, Yi; Published Date : 11 13 2013;11-13-; Source : J Am Chem Soc. 135(45):16805-16808 URL : https://stacks.cdc.gov/view/cdc/29812 Chooi, Yit-Heng et al. (2013). A Cytochrome P450 Serves as an Unexpected Terpene Cyclase during Fungal Meroterpenoid Biosynthesis. 135(45). Chooi, Yit-Heng et al. "A Cytochrome P450 Serves as an Unexpected Terpene Cyclase during Fungal Meroterpenoid Biosynthesis" 135, no. 45 (2013) Chooi, Yit-Heng et al. "A Cytochrome P450 Serves as an Unexpected Terpene Cyclase during Fungal Meroterpenoid Biosynthesis" vol. 135, no. 45, 2013 Export RIS Citation Information.

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Chooi, Yit-Heng ;

Hong, Young J.

11 13 2013 | J Am Chem Soc. 135(45):16805-16808

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Viridicatumtoxin (1) is a tetracycline-like fungal meroterpenoid with a unique, fused spirobicyclic ring system. Puzzlingly, no dedicated terpene cycl...
Epigenetic Genome Mining of an Endophytic Fungus Leads to Pleiotropic Biosynthesis of Natural Products

CITE Title : Epigenetic Genome Mining of an Endophytic Fungus Leads to Pleiotropic Biosynthesis of Natural Products Personal Author(s) : Mao, Xu-Ming;Xu, Wei;Li, Dehai;Yin, Wen-Bing;Chooi, Yit-Heng;Li, Yong-Quan;Tang, Yi;Hu, Youcai; Published Date : 6 22 2015;6-22-; Source : Angew Chem Int Ed Engl. 54(26):7592-7596 URL : https://stacks.cdc.gov/view/cdc/32930 Mao, Xu-Ming et al. (2015). Epigenetic Genome Mining of an Endophytic Fungus Leads to Pleiotropic Biosynthesis of Natural Products. 54(26). Mao, Xu-Ming et al. "Epigenetic Genome Mining of an Endophytic Fungus Leads to Pleiotropic Biosynthesis of Natural Products" 54, no. 26 (2015) Mao, Xu-Ming et al. "Epigenetic Genome Mining of an Endophytic Fungus Leads to Pleiotropic Biosynthesis of Natural Products" vol. 54, no. 26, 2015 Export RIS Citation Information.

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Mao, Xu-Ming ;

Xu, Wei

6 22 2015 | Angew Chem Int Ed Engl. 54(26):7592-7596

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The small-molecule biosynthetic potential of most filamentous fungi has remained largely unexplored and represents an attractive source for the discov...
Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition

CITE Title : Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition Personal Author(s) : Sato, Michio;Yagishita, Fumitoshi;Mino, Takashi;Uchiyama, Nahoko;Patel, Ashay;Chooi, Yit-Heng;Goda, Yukihiro;Xu, Wei;Noguchi, Hiroshi;Yamamoto, Tsuyoshi;Hotta, Kinya;Houk, Kendall N.;Tang, Yi;Watanabe, Kenji; Published Date : 11 2 2015;11-2-; Source : Chembiochem. 16(16):2294-2298 URL : https://stacks.cdc.gov/view/cdc/40002 Sato, Michio et al. (2015). Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition. 16(16). Sato, Michio et al. "Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition" 16, no. 16 (2015) Sato, Michio et al. "Involvement of Lipocalin-like CghA in Decalin-Forming Stereoselective Intramolecular [4+2] Cycloaddition" vol. 16, no. 16, 2015 Export RIS Citation Information.

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Sato, Michio ;

Yagishita, Fumitoshi

11 2 2015 | Chembiochem. 16(16):2294-2298

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Understanding enzymatic Diels-Alder (DA) reactions that can form complex natural product scaffolds is of considerable interest. Sch 210972 1, a potent...
by Partnering Thiohydrolase

CITE Title : by Partnering Thiohydrolase Personal Author(s) : Zabala, Angelica;O.;Chooi, Yit-Heng;Choi, Moon Seok;Lin, Hsiao-Ching;Tang, Yi; Published Date : May 29 2014 Source : ACS Chem Biol. 2014; 9(7):1576-1586. URL : https://stacks.cdc.gov/view/cdc/31448 Zabala, Angelica et al. (2014). by Partnering Thiohydrolase. 9(7). Zabala, Angelica et al. "by Partnering Thiohydrolase" 9, no. 7 (2014) Zabala, Angelica et al. "by Partnering Thiohydrolase" vol. 9, no. 7, 2014 Export RIS Citation Information.

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Zabala, Angelica ;

O.

May 29 2014 | ACS Chem Biol. 2014; 9(7):1576-1586.

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Fungal highly reducing polyketide synthases (HRPKSs) are an enigmatic group of multidomain enzymes that catalyze the biosynthesis of structurally dive...