Penicillium herquei is an anamorph, filamentous species of the genus of Penicillium which produces citreorosein, emodin, hualyzin, herquline B, janthinone, citrinin and duclauxin,.[1][3][4][5][6][7][8][9][10]
Further reading
- Robinson, N.; Wood, K.; Hylands, P. J.; Gibson, T. M.; Weedon, C. J.; Covill, N. (1992). "Blue Pigments of Penicillium herquei". Journal of Natural Products. 55 (6): 814–817. doi:10.1021/np50084a019.
- Marinho, A. M. R.; Marinho, P. S. B.; Santos, L. S.; Rodrigues Filho, E.; Ferreira, I. C. P. (2013). "Active polyketides isolated from Penicillium herquei". Anais da Academia Brasileira de Ciências. 85 (3): 909–12. doi:10.1590/S0001-37652013005000048. PMID 23969848.
- Marinho, A. M. D. R.; Marinho, P. C. S. B.; Rodrigues Filho, E. (2009). "Esteroides produzidos por Penicillium herquei, um fungo endofítico isolado dos frutos de Melia azedarach (Meliaceae)". Química Nova. 32 (7): 1710–1712. doi:10.1590/S0100-40422009000700005.
- Simpson, T. J. (1976). "Biosynthesis of deoxyherqueinone in Penicillium herquei from [13C]acetate and [13C]malonate. Assembly pattern of acetate into the phenalenone ring system". Journal of the Chemical Society, Chemical Communications (7): 258. doi:10.1039/C39760000258.
- Qiu, Y.; Niu, H.; Huang, W.; He, Y.; Wu, X. H. (2011). "Properties and secondary structure of tannase from Penicillium herquei". Biotechnology and Bioprocess Engineering. 16 (5): 858–866. doi:10.1007/s12257-011-0123-6.
- Tansakul, C.; Rukachaisirikul, V.; Maha, A.; Kongprapan, T.; Phongpaichit, S.; Hutadilok-Towatana, N.; Borwornwiriyapan, K.; Sakayaroj, J. (2014). "A new phenalenone derivative from the soil fungus Penicillium herqueiPSU-RSPG93". Natural Product Research. 28 (20): 1718–24. doi:10.1080/14786419.2014.941363. PMID 25079041.
- Chittreeya, Tansakul; Rukachaisirikul, Vatcharin; Atip, Maha; Thippaya, Kongprapan; Phongpaichit, Souwalak; Nongporn, Hutadilok-Towatana; Kawitsara, Borwornwiriyapan; Sakayaroj, Jariya (2014). "A new phenalenone derivative from the soil fungus Penicillium herquei PSU-RSPG93". Figshare. 28 (20): 1718–24. doi:10.1080/14786419.2014.941363. PMID 25079041.
- Enomoto, Y.; Shiomi, K.; Hayashi, M.; Masuma, R.; Kawakubo, T.; Tomosawa, K.; Iwai, Y.; Omura, S. (2010). "Chem Inform Abstract: Herquline B, a New Platelet Aggregation Inhibitor Produced by Penicillium herquei Fg-372". ChemInform. 27 (27): no. doi:10.1002/chin.199627238.
References
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^ a b c "Penicillium herquei". MycoBank. Retrieved 13 June 2016.
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^ Straininfo of Penicillium herquei
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^ "Taxonomy - Penicillium herquei". UniProt. Retrieved 13 June 2016.
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^ Ito, T; Yokoyama, E; Sato, H; Ujita, M; Funaguma, T; Furukawa, K; Hara, A (2003). "Xylosidases associated with the cell surface of Penicillium herquei IFO 4674". Journal of Bioscience and Bioengineering. 96 (4): 354–9. doi:10.1016/S1389-1723(03)90136-8. PMID 16233536.
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^ Marinho, A. M. R.; Marinho, P. S. B.; Santos, L. S.; Rodrigues Filho, E.; Ferreira, I. C. P. (2013). "Active polyketides isolated from Penicillium herquei". Anais da Academia Brasileira de Ciências. 85 (3): 909–12. doi:10.1590/S0001-37652013005000048. PMID 23969848.
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^ ATCC
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^ Bryant, F. O.; Cutler, H. G.; Jacyno, J. M. (1993). "Properties and cost effective method for production of the antitumor agent declauxin from sporulating Penicillium herquei". Journal of Pharmaceutical Sciences. 82 (12): 1214–7. doi:10.1002/jps.2600821206. PMID 8308698.
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^ Ding, L; Fotso, S; Li, F; Qin, S; Laatsch, H (2008). "Hualyzin, a symmetrical urea derivative isolated from Penicillium herquei isolate GA4". Journal of Natural Products. 71 (6): 1068–9. doi:10.1021/np700751b. PMID 18479164.
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^ Omura, S; Hirano, A; Iwai, Y; Masuma, R (1979). "Herquline, a new alkaloid produced by Penicillium herquei. Fermentation, isolation and properties". The Journal of Antibiotics. 32 (8): 786–90. doi:10.7164/antibiotics.32.786. PMID 500499.
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^ Enomoto, Y; Shiomi, K; Hayashi, M; Masuma, R; Kawakubo, T; Tomosawa, K; Iwai, Y; Omura, S (1996). "Herquline B, a new platelet aggregation inhibitor produced by Penicillium herquei Fg-372". The Journal of Antibiotics. 49 (1): 50–3. doi:10.7164/antibiotics.49.50. PMID 8609085.
