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. 2004 May;135(1):95–102. doi: 10.1104/pp.103.037051

Table III.

Relative activity of purified native and recombinant POMTs with various substrates

Native POMT Recombinant POMT
graphic file with name fx1.jpg Orcinol (R : OH) 2.4 ± 0.07 1.5 ± 0.08
3-Methoxy, 5-hydroxy toluene (R : OCH3) 0 0
graphic file with name fx2.jpg Phloroglucinol (R1=R2 : OH) 100 100
3,5-Dihydroxyanisole (R1 : OH, R2 : OCH3) 1.7 ± 0.05 1.8 ± 0.03
3,5-Dimethoxyphenol (R1=R2 : OCH3) 0 0
graphic file with name fx3.jpg Resorcinol (R : OH) 32.9 ± 1.6 20.7 ± 1.5
3-Methoxyphenol (R : OCH3) 0 0
Phenol (R : H) 0 0
graphic file with name fx4.jpg Catechol (R : H) 0 0
4-Methyl catechol (R : CH3) 0 0
Caffeic acid (R : CH=CHCOOH) 0 0
graphic file with name fx5.jpg 2-Methoxyphenol (R : H) 0 0
2-Methoxy, 4-methylphenol (R : CH3) 0 0
Isoeugenol (R : CH=CHCH3) 0 0
Eugenol (R : CH2CH=CH2) 0 0

The activity with PLG as a substrate was set to 100.