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              Possible digestive function of lysozyme in a wood-feeding termite,
              Reticulitermes speratus 
              A. Fujita 1 , 
              I. Shimizu 1 & T. Abe 1 
              1 Center for 
              Ecological Research, Kyoto Univ., Hiranocho, Kamitanakami, Otsu, 
              Shiga 520-2113, Japan 
                Lysozyme catalyzes 
                the hidrolysis of the 1, 4-B-gucosidic linkage between N-acetylmuramic 
                acid and N-acetylglucosamine of peptidoglucan present in the 
                cell wall of many bacteria, causing cell lysis. Lysozyme is part 
                of the defense mechanism against bacteria and has been 
                distributed in most animals, including insects. Lysozyme has 
                also implied in the midgut digestion of bacteria by organisms 
                which ingest large amounts of them, or that harbor a bacterial 
                culture in their guts, exemplified by vertebrate foregut 
                fermenters Similarly, among the insects, digesting lysozymes are 
                reported from saprophagous Diptera. These insects lysis bacteria 
                in their food with stomach lysozyme and absorb microbial tissue 
                in the midgut. On the other hand, wood-feeding termites re also 
                oligonitrotrophic, and possibility that how they get enough 
                nitrogen to construct living body is intriguing. We suspected 
                the possibility that termites have digestive lysozyme to utilize 
                their hindgut bacteria as nutrient source. We measured lysozyme 
                and protease activities of enzyme extract prepared from termite 
                tissues. Using amino acid analyzer, we analyzed amino acid 
                composition in the termite guts, and calculated the 
                concentration of total free amino acid in each part of guts. 
                Total activity of lysozyme was found predominantly in salivary 
                gland and to a minor extent in digestive tract. However, high 
                specific activity of lysozyme was detected in foregut as well as 
                in salivary gland. The similarity of lysozyme pH-profile in 
                salivary gland and foregut suggested that foregut lysozyme came 
                from salivary gland. The highest protease activity having the 
                optimum pH 7.5 was found in midgut. Total amino acid content and 
                concentration of midgut ware higher than foregut and hindgut. 
                From these results, the possibility that lysozyme secreted from 
                salivary gland to foregut digest the symbiont bacteria 
                transferred by trophallaxis of the termite for use of nitrogen 
                source is suggested. Provided that termites utilized their 
                hindgut bacteria, it would be reasonable for them to ingest gut 
                bacteria through proctodeal trophallaxis and lysis them in their 
                foreguts, because their fermentative tissue is hindgut. 
                Although, Breznak suspected the possibility of nutritive 
                potential of bacterial cell material through trophallaxis in 
                termites, there has been no study on this problem. In this 
                study, we observed the behavior of R. speratus, and 
                indicate termites digest a part of hindgut bacteria as nitrogen 
                resource through proctodeal trophallaxis in the enzymologic way. Index terms:
                Reticulitermes speratus, Lysozyme, Trophallaxis, Nitrogen 
                Metabolism 
 
                  
                  Copyright: The copyrights of 
                  this abstract belong to the author (see right-most box of 
                  title table). This document also appears in Session 13 – 
                  INSECT PHISIOLOGY, NEUROSCIENCES, IMMUNITY AND CELL BIOLOGY 
                  Symposium and Poster Session, ABSTRACT BOOK II – 
                  XXI-International Congress of Entomology, Brazil, August 
                  20-26, 2000.   |