참고문헌
- Im K, Kim J, Min H. Ginseng, the natural effectual antiviral: protective effects of Korean Red Ginseng against viral infection. J Ginseng Res 2016;40:309-14. https://doi.org/10.1016/j.jgr.2015.09.002
- Lee SM, Bae BS, Park HW, Ahn NG, Cho BG, Cho YL, Kwak YS. Characterization of Korean red ginseng (Panax ginseng Meyer): history, preparation method, and chemical composition. J Ginseng Res 2015;39:384-91. https://doi.org/10.1016/j.jgr.2015.04.009
- Hussain A, Bose S, Wang JH, Yadav MK, Mahajan GB, Kim H. Fermentation, a feasible strategy for enhancing bioactivity of herbal medicines. Food Res Inter 2016;81:1-16. https://doi.org/10.1111/1750-3841.13023
- Lee SH, Oh M, Park J, Jang SY, Cheong SH, Lee H, Moon SH. Antioxidant and anti-inflammatory activities of the ethanolic extract of fermented red ginseng marc. Food Sci Biotechnol 2015;24:651-7. https://doi.org/10.1007/s10068-015-0085-0
- Li Z, Ahn HJ, Kim NY, Lee YN, Ji GE. Korean ginseng berry fermented by mycotoxin non-producing Aspergillus Niger and Aspergillus oryzae: ginsenoside analyses and anti-proliferative activities. Biol Pharm Bull 2016;39:1461-7. https://doi.org/10.1248/bpb.b16-00239
- Fatima N, Muhammad SA, Khan I, Qazi MA, Shahzadi I, Mumtaz A, Hashmi MA, Khan AK, Ismail T. Chaetomium endophytes: a repository of pharmacologically active metabolites. Acta Physiol Plant 2016;38:136. https://doi.org/10.1007/s11738-016-2138-2
- Zhou ZF, Menna M, Cai YS, Guo YW. Polyacetylenes of marine origin: chemistry and bioactivity. Chem Rev 2015;115:1543-96. https://doi.org/10.1021/cr4006507
- Negri R. Polyacetylenes from terrestrial plants and fungi: recent phytochemical and biological advances. Fitoterapia 2015;106:92-109. https://doi.org/10.1016/j.fitote.2015.08.011
- Satoh M, Ishii M, Watanabe M, Isobe K, Uchiyama T, Fujimoto Y. Absolute structure of panaxytriol. Chem Pharm Bull 2002;50:126-8. https://doi.org/10.1248/cpb.50.126
- Chou TC, Dong HJ, Zhang XG, Lei XG, Hartung J, Zhang YD, Lee JH, Wilson RM, Danishefsky SJ. Multifaceted cytoprotection by synthetic polyacetylenes inspired by the ginseng-derived natural product, panaxytriol. Proc Natl Acad Sci USA 2011;108:14336-41. https://doi.org/10.1073/pnas.1111332108
-
Swizdor A. Baeyer-Villiger oxidation of some
$C_{19}$ steroids by Penicillium lanosocoeruleum. Molecules 2013;18:13812-22. https://doi.org/10.3390/molecules181113812 - Rieser MJ, Kozlowski JF, Wood KV, McLaughlin JL. Muricatacin : a simple biologically active acetogenin derivative from the seeds of Annona muricata (Annonaceae). Tetrahedron Lett 1991;32:1137-40. https://doi.org/10.1016/S0040-4039(00)92027-6
- Gurjar MK, Kumar VS, Rao BV. Synthesis of a new type of antitumour agent panaxytriol: synthesisof its four diastereomers.Tetrahedron1999;55:12563-76. https://doi.org/10.1016/S0040-4020(99)00732-2
- Winter JM, Cascio D, Dietrich D, Sato M, Watanabe K, Sawaya MR, Vederas JC, Tang Y. Biochemical and structural basis for controlling chemical modularity in fungal polyketide biosynthesis. J Am Chem Soc 2015;137:9885-93. https://doi.org/10.1021/jacs.5b04520
- Yasuhide M, Yamada T, Numata A, Tanaka R. Chaetomugilins, new selectively cytotoxic metabolites, produced by a marine fish-derived Chaetomium species. J Antibiot 2008;61:615-22. https://doi.org/10.1038/ja.2008.81
- Tao SJ, Wang Y, Zhang X, Guan SH, Guo DA. Biotransformation of gambogenic acid by Chaetomium globosum CICC 2445. Nat Prod Comm 2012;7:197-8.
- Dong XR, Gao ZH, Hu HX, Gao RR, Sun D. Microbial transformation of pseudoprotodioscin by Chaetomium olivaceum. J Mol Catal B: Enzym 2016;130:88-95. https://doi.org/10.1016/j.molcatb.2016.05.001
피인용 문헌
- Inducing Intermediates in Biotransformation of Natural Polyacetylene and A Novel Spiro-γ-Lactone from Red Ginseng by Solid Co-Culture of Two Gut Chaetomium globosum and The Potential Bioactivi vol.25, pp.5, 2020, https://doi.org/10.3390/molecules25051216