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. 2009 Dec 14;3(1):192–211. doi: 10.1093/mp/ssp098

Table 2.

In vitro screening of heterologously expressed UGTs that showed the most significant changes in expression level between sur2 knock-out mutant and wild-type towards a set of six commercially available indole and phenylpropanoid compounds.

Name Group S1 S2 S3 S4 S5 S6
UGT73B2* D +++ (+) (+) ++ + (+)
UGT73B3 D (+) +++ (+) (+)
UGT73B5 D (+) (+)
UGT72B1 E (+) (+) +++
UGT72E2 E (+)
UGT71C3* E +++ + ++ (+)
UGT74F1 L +++ (+) (+) ++ (+)
UGT75B1 L +++ +++ (+) +++
UGT84A2 L +++ (+) (+) ++ +++
UGT84A3 L ++ (+) (+) +++

S1: indole-3-carboxylic acid; S2: indole-3-acetic acid; S3: indole-3-carboxaldehyde; S4: coniferyl alcohol; S5: sinapoyl-alcohol; S6: sinapic acid.

* UGTs that were not identified based on their direct up-regulation, but were selected because of their homology to other up-regulated UGTs (Table 3). Based on the intensity of the signal corresponding to the formation of a glucosylated product, a relative scale was established: +++: high conversion; ++: medium conversion; +: low conversion; (+): minute conversion; -: no conversion.