1% SDS) at constant voltage (200 V) for 30 min. Gels were stained with Oriole™ Fluorescent Gel Stain (Bio-Rad®) and viewed under UV light to determine the presence of protein bands. APRO© SP-2110 Broad Range ladder (APRO Life Science Institute Inc., Naruto city, Tokushima, Japan) was used to estimate molecular weight. Proteins on SDS–PAGE gels were transferred to a Sequi-Blot™ polyvinylidene fluoride (PVDF) membrane (Bio-Rad) using a semi-dry transfer cell as per

Hirano and Watanabe (1990). The transblotted membrane was blocked with Blocking One solution (Nacalai Tesque Inc., Kyoto, Japan) and applied with anti-A18 mutant endogenous termite cellulase rabbit serum (Tokuda et al., 2012) diluted 1:1000 in Solution 1 of the Can Get Signal® immunoreaction enhancer solution kit (Toyobo Co., Ltd, JAK inhibitor Osaka, Japan). Following washing with TPBS (phosphate-buffered saline with 0.01% Tween 20), the membrane was applied with goat anti-rabbit IgG-horseradish peroxidase conjugate (Santa Cruz Biotechnology Inc, CA, USA) followed by TPBS washing. Applications of blocking solution and both antisera were conducted with a Snap i.d.™ protein detection system (EMD Millipore, Sirolimus datasheet Billerica, MA, USA). Before vacuum-application of the antiserum solutions onto a PVDF membrane, the solution was incubated with agitation on the membrane for 10 min at room temperature.

Finally, presence of antigen on the membrane was visualized by incubation with 3,3′,5,5′-tetramethylbenzidine solution (T0565, Sigma). APRO SP-2110 Broad Range protein ladder was used as a negative control for the primary and secondary anti-sera. For a positive control for the second anti-serum, a protein ladder with IgG binding sites (MagicMark™ XP Western Protein Standard, Life Technologies) was employed. The volumes of the foregut and the midgut of a typical, full-grown, male E. calcarata averaged 3.0 and 777 mL, respectively. EG concentration of the

foregut and the first, second, and third sections of the midgut were 4.1, 20.9, 2.0, and 0 (not detected) units/mL, respectively ( Fig. 2). A unit is defined PFKL as the amount of enzyme that produces one μmole of reducing sugar per minute from CMC in the TZB method ( Calderón-Cortés et al., 2010). These findings support the hypothesis that digestive activity is concentrated in the anterior midgut, whose pleating and folding might slow down passage of food debris to increase digestibility. The role of the appendices of the posterior midgut is likely not enzyme production, as cellulase activity stops after the anterior midgut. The phasmid cellulase concentrations were relatively low compared with the exceptionally high midgut concentrations (>1000 units/mL) found in some termite species ( Tokuda et al., 2004 and Tokuda et al., 2005), but are still significant. An EG protein was isolated by hydrophobicity interaction chromatography using a HiTrap Phenyl FF (low sub) column. The protein was eluted as three separate peaks at different concentrations of ammonium sulfate (1, 0.