메뉴 건너뛰기




Volumn 64, Issue 12, 2018, Pages 4182-4186

Identification of the pyranonigrin A biosynthetic gene cluster by genome mining in Penicillium thymicola IBT 5891

Author keywords

biosynthesis; genome mining; heterologous expression; pyranonigrin A

Indexed keywords


EID: 85056396287     PISSN: 00011541     EISSN: 15475905     Source Type: Journal    
DOI: 10.1002/aic.16324     Document Type: Article
Times cited : (23)

References (22)
  • 1
    • 45849086857 scopus 로고    scopus 로고
    • Antioxidative pyranonigrins in rice mold starters and their suppressive effect on the expression of blood adhesion molecules
    • Miyake Y, Mochizuki M, Ito C, Itoigawa M, Osawa T. Antioxidative pyranonigrins in rice mold starters and their suppressive effect on the expression of blood adhesion molecules. Biosci Biotechnol Biochem. 2008;72:1580-1585
    • (2008) Biosci Biotechnol Biochem , vol.72 , pp. 1580-1585
    • Miyake, Y.1    Mochizuki, M.2    Ito, C.3    Itoigawa, M.4    Osawa, T.5
  • 2
    • 4644243337 scopus 로고    scopus 로고
    • New natural products from the sponge-derived fungus Aspergillus niger
    • Hiort J, Maksimenka K, Reichert M, et al. New natural products from the sponge-derived fungus Aspergillus niger. J Nat Prod. 2004;67:1532-1543
    • (2004) J Nat Prod , vol.67 , pp. 1532-1543
    • Hiort, J.1    Maksimenka, K.2    Reichert, M.3
  • 3
    • 34548036029 scopus 로고    scopus 로고
    • Reassessing the structure of pyranonigrin
    • Schlingmann G, Taniguchi T, He H, et al. Reassessing the structure of pyranonigrin. J Nat Prod. 2007;70:1180-1187
    • (2007) J Nat Prod , vol.70 , pp. 1180-1187
    • Schlingmann, G.1    Taniguchi, T.2    He, H.3
  • 4
    • 85017663496 scopus 로고    scopus 로고
    • Elucidation of biosynthetic pathways of natural products
    • Kishimoto S, Tsunematsu Y, Sato M, Watanabe K. Elucidation of biosynthetic pathways of natural products. Chem Rec. 2017;17:1095-1108
    • (2017) Chem Rec , vol.17 , pp. 1095-1108
    • Kishimoto, S.1    Tsunematsu, Y.2    Sato, M.3    Watanabe, K.4
  • 5
    • 36148966180 scopus 로고    scopus 로고
    • Isolation of the antioxidant pyranonigrin-A from rice mold starters used in the manufacturing process of fermented foods
    • Miyake Y, Ito C, Itoigawa M, Osawa T. Isolation of the antioxidant pyranonigrin-A from rice mold starters used in the manufacturing process of fermented foods. Biosci Biotechnol Biochem. 2007;71:2515-2521
    • (2007) Biosci Biotechnol Biochem , vol.71 , pp. 2515-2521
    • Miyake, Y.1    Ito, C.2    Itoigawa, M.3    Osawa, T.4
  • 6
    • 84889608086 scopus 로고    scopus 로고
    • Pyranonigrin E: a PKS-NRPS hybrid metabolite from Aspergillus niger identified by genome mining
    • Awakawa T, Yang XL, Wakimoto T, Abe I. Pyranonigrin E: a PKS-NRPS hybrid metabolite from Aspergillus niger identified by genome mining. Chembiochem. 2013;14:2095-2099
    • (2013) Chembiochem , vol.14 , pp. 2095-2099
    • Awakawa, T.1    Yang, X.L.2    Wakimoto, T.3    Abe, I.4
  • 7
    • 84944886728 scopus 로고    scopus 로고
    • Elucidation of pyranonigrin biosynthetic pathway reveals a mode of Tetramic acid, fused γ-pyrone, and exo-methylene formation
    • Yamamoto T, Tsunematsu Y, Noguchi H, Hotta K, Watanabe K. Elucidation of pyranonigrin biosynthetic pathway reveals a mode of Tetramic acid, fused γ-pyrone, and exo-methylene formation. Org Lett. 2015;17:4992-4995
    • (2015) Org Lett , vol.17 , pp. 4992-4995
    • Yamamoto, T.1    Tsunematsu, Y.2    Noguchi, H.3    Hotta, K.4    Watanabe, K.5
  • 8
    • 84896845229 scopus 로고    scopus 로고
    • Studies on pyranonigrins-isolation of pyranonigrin E and biosynthetic studies on pyranonigrin A
    • Riko R, Nakamura H, Shindo K. Studies on pyranonigrins-isolation of pyranonigrin E and biosynthetic studies on pyranonigrin A. J Antibiot (Tokyo). 2014;67:179-181
    • (2014) J Antibiot (Tokyo) , vol.67 , pp. 179-181
    • Riko, R.1    Nakamura, H.2    Shindo, K.3
  • 9
    • 84871486514 scopus 로고    scopus 로고
    • Molecular diversity sculpted by fungal PKS-NRPS hybrids
    • Boettger D, Hertweck C. Molecular diversity sculpted by fungal PKS-NRPS hybrids. Chembiochem. 2013;14:28-42
    • (2013) Chembiochem , vol.14 , pp. 28-42
    • Boettger, D.1    Hertweck, C.2
  • 10
    • 85041474743 scopus 로고    scopus 로고
    • Biosynthesis of long-chain N-acyl amide by a truncated polyketide synthase-nonribosomal peptide Synthetase hybrid Megasynthase in fungi
    • Hai Y, Tang Y. Biosynthesis of long-chain N-acyl amide by a truncated polyketide synthase-nonribosomal peptide Synthetase hybrid Megasynthase in fungi. J Am Chem Soc. 2018;140:1271-1274
    • (2018) J Am Chem Soc , vol.140 , pp. 1271-1274
    • Hai, Y.1    Tang, Y.2
  • 11
    • 84960075421 scopus 로고    scopus 로고
    • Comprehensive curation and analysis of fungal biosynthetic gene clusters of published natural products
    • Li YF, Tsai KJS, Harvey CJB, et al. Comprehensive curation and analysis of fungal biosynthetic gene clusters of published natural products. Fungal Genet Biol. 2016;89:18-28
    • (2016) Fungal Genet Biol , vol.89 , pp. 18-28
    • Li, Y.F.1    Tsai, K.J.S.2    Harvey, C.J.B.3
  • 12
    • 85042365902 scopus 로고    scopus 로고
    • Recent advances in reconstructing microbial secondary metabolites biosynthesis in Aspergillus spp
    • He Y, Wang B, Chen W, Cox RJ, He J, Chen F. Recent advances in reconstructing microbial secondary metabolites biosynthesis in Aspergillus spp. Biotechnol Adv. 2018;36:739-783
    • (2018) Biotechnol Adv , vol.36 , pp. 739-783
    • He, Y.1    Wang, B.2    Chen, W.3    Cox, R.J.4    He, J.5    Chen, F.6
  • 13
    • 84895075667 scopus 로고    scopus 로고
    • Strategies for mining fungal natural products
    • Wiemann P, Keller NP. Strategies for mining fungal natural products. J Ind Microbiol Biotechnol. 2014;41:301-313
    • (2014) J Ind Microbiol Biotechnol , vol.41 , pp. 301-313
    • Wiemann, P.1    Keller, N.P.2
  • 14
    • 84928492275 scopus 로고    scopus 로고
    • Tandem prenyltransferases catalyze isoprenoid elongation and complexity generation in biosynthesis of quinolone alkaloids
    • Zou Y, Zhan Z, Li D, et al. Tandem prenyltransferases catalyze isoprenoid elongation and complexity generation in biosynthesis of quinolone alkaloids. J Am Chem Soc. 2015;137:4980-4983
    • (2015) J Am Chem Soc , vol.137 , pp. 4980-4983
    • Zou, Y.1    Zhan, Z.2    Li, D.3
  • 16
    • 80052828266 scopus 로고    scopus 로고
    • A new class of IMP dehydrogenase with a role in self-resistance of mycophenolic acid producing fungi
    • Hansen BG, Genee HJ, Kaas CS, et al. A new class of IMP dehydrogenase with a role in self-resistance of mycophenolic acid producing fungi. BMC Microbiol. 2011;11:202
    • (2011) BMC Microbiol , vol.11 , pp. 202
    • Hansen, B.G.1    Genee, H.J.2    Kaas, C.S.3
  • 17
    • 84954557172 scopus 로고    scopus 로고
    • Identification and functional analysis of the mycophenolic acid gene cluster of Penicillium roqueforti
    • Del-Cid A, Gil-Durán C, Vaca I, et al. Identification and functional analysis of the mycophenolic acid gene cluster of Penicillium roqueforti. PLoS One. 2016;11:e0147047
    • (2016) PLoS One , vol.11
    • Del-Cid, A.1    Gil-Durán, C.2    Vaca, I.3
  • 19
    • 85018462166 scopus 로고    scopus 로고
    • Integration of chemical, genetic, and bioinformatic approaches delineates fungal polyketide-peptide hybrid biosynthesis
    • Yokoyama M, Hirayama Y, Yamamoto T, Kishimoto S, Tsunematsu Y, Watanabe K. Integration of chemical, genetic, and bioinformatic approaches delineates fungal polyketide-peptide hybrid biosynthesis. Org Lett. 2017;19:2002-2005
    • (2017) Org Lett , vol.19 , pp. 2002-2005
    • Yokoyama, M.1    Hirayama, Y.2    Yamamoto, T.3    Kishimoto, S.4    Tsunematsu, Y.5    Watanabe, K.6
  • 21
    • 67650649489 scopus 로고    scopus 로고
    • IMP dehydrogenase: structure, mechanism, and inhibition
    • Hedstrom L. IMP dehydrogenase: structure, mechanism, and inhibition. Chem Rev. 2009;109:2903-2928
    • (2009) Chem Rev , vol.109 , pp. 2903-2928
    • Hedstrom, L.1
  • 22
    • 39549088916 scopus 로고    scopus 로고
    • Inosine monophosphate dehydrogenase (IMPDH) as a target in drug discovery
    • Shu Q, Nair V. Inosine monophosphate dehydrogenase (IMPDH) as a target in drug discovery. Med Res Rev. 2008;28:219-232
    • (2008) Med Res Rev , vol.28 , pp. 219-232
    • Shu, Q.1    Nair, V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.