Hinokiresinol is not a precursor of agatharesinol in the norlignan biosynthetic pathway in Japanese cedar
Tài liệu tham khảo
Berry, 1996, Labeled compounds of interest as antitumour agents-V. Syntheses of [18O]-5-methylisoquinolinone and 1-(furan-2-yl-[18O]-methoxy)-5-methyl-isoquinoline, J Label Compd Radiopharm, 38, 935, 10.1002/(SICI)1099-1344(199610)38:10<935::AID-JLCR904>3.0.CO;2-2
Erdtman, 1979, Phenolic and terpenoid heartwood constituents of Libocedrus yateensis, Phytochemistry, 18, 1495, 10.1016/S0031-9422(00)98482-6
Imai, 2005, Induction of the biosynthesis of agatharesinol, a norlignan, in sapwood sticks of Cryptomeria japonica under humidity-regulated circumstance, J Wood Sci, 51, 537, 10.1007/s10086-004-0675-6
Imai, 2006, Evidence for involvement of the phenylpropanoid pathway in the biosynthesis of the norlignan agatharesinol, J Plant Physiol, 163, 483, 10.1016/j.jplph.2005.08.009
Luderitz, 1981, Enzymatic synthesis of lignin precursors. Comparison of cinnamoyl-CoA reductase and cinnamyl alcohol: NADP+ dehydrogenase from spruce (Picea abies L.) and soybean (Glycine max L.), Eur J Biochem, 119, 115, 10.1111/j.1432-1033.1981.tb05584.x
Miyoshi M, Fujita K, Sakai K. Studies on the biosynthesis of hinokiresinol using suspension cultured cells of Cryptomeria japonica. Abstracts of the 50th annual meeting of the Japan Wood Research Society, 2000. p. 423.
Muraoka O, Zheng B-Z, Fujiwara N, Tanabe G. Enantioselective total synthesis of the di-O-methyl ethers of (−)-agatharesinol, (+)-hinokiresinol and (−)-sugiresinol, characteristic norlignans of Coniferae. J Chem Soc, Perkin Trans I 1995; 405–11.
Noguchi M, Tahara M, Sakai K. The biosynthesis of norlignans in softwood suspension cultured cells. Abstracts of the 47th annual meeting of the Japan Wood Research Society, 1997. p. 496.
Sarni, 1984, Purification and properties of cinnamoyl-CoA reductase and cinnamyl alcohol dehydrogenase from poplar stems (Populus X euramericana), Eru J Biochem, 139, 259, 10.1111/j.1432-1033.1984.tb08002.x
Suzuki S, Umezawa T, Shimada M. Norlignan biosynthesis in Asparagus officinalis L.: the norlignan originated from two non-identical phenylpropane units. J Chem Soc, Perkin Trans I 2001;3252–7.
Suzuki S, Nakatsubo T, Umezawa T, Shimada M. First norlignan in vitro formation with Asparagus officinalis enzyme preparation. Chem Commun 2002;1088–9.
Suzuki S, Yamamura M, Shimada M, Umezawa T. A heartwood norlignan, (E)-hinokiresinol, is formed from 4-coumaryl 4-coumarate by a Cryptomeria japonica enzyme preparation. Chem Commun 2004:2838–9.
Yamamura M, Suzuki S, Nakatsubo T, Hattori T, Shimada M, Umezawa T. cDNA cloning of Asparagus officinalis hinokiresinol synthase. In: Proceedings of the International Symposium on Wood Science and Technology, Yokohama, vol. 2, 2005. p. 345–6.
