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. 2007 Mar;143(3):1372–1384. doi: 10.1104/pp.106.090811

Table I.

TAG lipase activity of recombinant fusion proteins MBP-LipF and MBP-LipS

Lipase activity was measured by iodine-stained TLC and a NEFA-C assay. Values are means ± se for n = 3. Means identified by different superscripts are significantly different at the 5% level based on Duncan's multiple range test. Percentages relative to the pMal-c2 control are indicated. MBP, Maltose binding protein control produced from the empty pMal-c2 vector; MBP-lipF, full-length lipase fused to MBP; MBP-lipS, truncated lipase (lacking predicted transit peptide) fused to MBP.

Recombinant Protein TLC Assay
NEFA-C Assay
Density Relative to Background × 104 % Increase mmol FFA/μg Protein % Increase
MBP 8.50a ± 0.30 23.3a ± 2.04
MBP-lipF 9.17a ± 0.30 7.9 26.0a,b ± 2.06 11.3
MBP-lipS 11.0b ± 0.05 29.5 33.3b ± 1.79 42.5