Phasmids are also the only insect order composed entirely of obligate herbivores (Calderón-Cortés et al., 2012). These factors suggest a unique digestive metabolism compared to their closest evolutionary relatives among the Polyneoptera, thought to be either the omnivorous Orthoptera (Flook and Rowell, 1998), carnivorous Notoptera (Arillo and Engel, 2006), or the herbivorous/detritivorous Embioptera (Terry and Whiting, 2005). Comparative analysis of cellulase enzymes

[if present] in these orders could Rucaparib research buy help resolve the current polytomy in that branch of the insect phylogeny (Gullan and Cranston, 2010). Phasmids are also relatively large and easy to rear (Brock, 2003), plus several species are parthenogenetic, which increases their suitability for genetic modeling research (Tuccini et al., 1996). The Phasmatodea midgut, though of a uniform diameter, is differentiated into a muscular and pleated anterior section, a posterior section with the enigmatic appendices of the midgut (de Sinéty, 1901 and Ramsay, 1955), and an undifferentiated space in between (Fig. 1). The function of the appendices – long filaments attached to the MK2206 midgut via pyriform ampules – is unknown, though they have been hypothesized to either be secretory or excretory. The surface area of the anterior midgut lumen is increased by its pleating,

which might slow down the speed of passage of food debris. This would increase digestibility as cellulose digestion is a relatively time consuming process due to its insolubility and tight structure (Mason, 1994 and Silk, 1989). For this study, we chose to examine EG’s due to their importance

in primary breakdown of cellulose in animals, and Phasmatodea as they are obligate leaf-eaters from whom no cellulases have ever been recovered. Their phylogenetic placement (Davison and Blaxter, 2005) and the lack of microbial symbionts in their midgut (Shelomi et al., 2013) suggests phasmids produce endogenous GH9 EGs. We hypothesized that cellulase activity would be highest in the anterior midgut and lower in the posterior, suggesting polysaccharide breakdown occurs in the anterior midgut and glucose absorption in the posterior midgut. We focused on the giant new guinea walking stick, Eurycantha calcarata (Phasmatidae: OSBPL9 Eurycanthinae), for proteomic analysis due to its large size providing more tissue for analysis per insect and facilitating volumetric analysis of the digestive tract. Genetic analysis was also performed on a distantly related, common Japanese walking stick Entoria okinawaensis (Phasmatidae: Clitumninae) to explore the distribution of orthologous cellulase genes in Phasmatodea. E. calcarata adults were lab-reared at the Bohart Museum of Entomology (Davis, CA, USA) at room temperature and fed Quercus sp. leaves. Only males were used.