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1 oxy-oleanane (12,13beta-epoxy-16beta-hydroxy-beta-amyrin).
2 ) and the isomers (lupeol, alpha-amyrin, and beta-amyrin).
3 ading to the accumulation of 16alpha-hydroxy beta-amyrin.
4 on products, including the simple triterpene beta-amyrin.
5  are synthesized from the simple triterpene, beta-amyrin.
6  beta-Amyrin acetate (1), n-octacosanol (2), beta-Amyrin (3), stigmasterol (4), xanthyletin (6), allo
7 These aglycones are most likely derived from beta-amyrin, a product of the cyclization of 2,3-oxidosq
8                                              beta-Amyrin accumulated solely in the intracuticular wax
9                                              beta-Amyrin acetate (1), n-octacosanol (2), beta-Amyrin
10 aromyces cerevisiae led to the production of beta-amyrin and alpha-amyrin, the direct precursors of o
11 served for the contrasting environments, and beta-amyrin and cholesterol were more predominant in the
12 d alpha- and beta-amyrin synthase, and mixed beta-amyrin and friedelin synthase activities.
13 l (-)-achilleol B, camelliol A, and (+)-seco-beta-amyrin as minor compounds.
14 synthase that produced both alpha-amyrin and beta-amyrin but had a product preference for alpha-amyri
15                Oat roots also synthesize the beta-amyrin-derived triterpene glycoside avenacin A-1, w
16       The accumulation of elevated levels of beta-amyrin in these mutants triggers a "superhairy" roo
17  synthase that converts 2,3-oxidosqualene to beta-amyrin in yeast, and its role in maesasaponin biosy
18 YP87D16 catalyses the C-16alpha oxidation of beta-amyrin in yeast, leading to the accumulation of 16a
19                            The metabolism of beta-amyrin is blocked in sad2 mutants, which therefore
20                                              beta-Amyrin is present at low levels in the roots of dip
21 t, CYP716A75 catalyses the C-28 oxidation of beta-amyrin, leading to the accumulation of mainly eryth
22                              The function of beta-amyrin per se is unknown, but this molecule can ser
23                            When expressed in beta-amyrin-producing yeast, CYP716A75 catalyses the C-2
24                      sad2 mutants accumulate beta-amyrin, suggesting that they are blocked early in t
25  synthase (SS), squalene epoxidase (SE), and beta-amyrin synthase (beta-AS).
26 nctional interconversion between pentacyclic beta-amyrin synthase (CqbAS1) and B,C-ring-opened triter
27                 Three full-length OSC cDNAs, beta-amyrin synthase (WsOSC/BS), lupeol synthase (WsOSC/
28 ) in even evolutionarily distant Arabidopsis beta-amyrin synthase could generate quinoxides, indicati
29                                   MlbAS is a beta-amyrin synthase that converts 2,3-oxidosqualene to
30 ynthase gene AtLUP4 (for lupeol synthase4 or beta-amyrin synthase) to compare water loss with and wit
31 zymes with lupeol synthase, mixed alpha- and beta-amyrin synthase, and mixed beta-amyrin and friedeli
32                    ObAS1 was identified as a beta-amyrin synthase, whereas ObAS2 was a mixed amyrin s
33  production of the major triterpene scaffold beta-amyrin, the precursor of erythrodiol, oleanolic and
34                                              Beta-amyrin was the sole product of the cyclization of s
35 hree triterpenols (lupeol, alpha-amyrin, and beta-amyrin) were chosen as the analytes.