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. 2001 Jul 3;98(15):8909–8914. doi: 10.1073/pnas.141239398

Table 1.

Identification of the metabolites from GAs incubated with recombinant rice GA 3β-hydroxylases by full-scan GC-MS and Kovats retention indices (KRI)

Recombinant protein Substrate GA Product GA* KRI Characteristic ions at m/z (% relative intensity of base peak)
OsGA3ox1 2H3-GA9 GA4 2610 479 (17), 464 (31), 389 (36), 227 (100)
GA7 2627 477 (4), 462 (11), 389 (6), 225 (100)
GA34 2750 567 (100), 552 (14), 477 (4), 232 (18)
2H2-GA20 GA1 2748 566 (100), 551 (31), 449 (33), 209 (25)
GA3 2766 564 (100), 549 (42), 447 (26), 210 (48)
GA8 2880 654 (13), 639 (5), 537 (100), 313 (11)
2H0-GA5 GA3 2768 562 (100), 547 (47), 445 (38), 208 (79)
2H2-GA44 GA38 2939 522 (73), 507 (6), 432 (5), 209 (100)
OsGA3ox2 2H3-GA9 GA4 2608 479 (12), 464 (21), 389 (25), 227 (100)
2H2-GA20 GA1 2745 566 (100), 551 (30), 449 (60), 209 (45)
2H0-GA5 GA3 2766 562 (87), 547 (38), 445 (48), 208 (100)
2H2-GA44 GA38 2940 522 (84), 507 (8), 432 (4), 209 (100)
*

For the identification of GA38, the sample was derivatized to the methyl ester trimethylsilyl ether. Other samples were trimethylsilylated.