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Microsomal marker enzymes of Manduca sexta (L) midgut
Author(s) -
Weirich Gunter F.,
Adams Jean R.
Publication year - 1984
Publication title -
archives of insect biochemistry and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.576
H-Index - 66
eISSN - 1520-6327
pISSN - 0739-4462
DOI - 10.1002/arch.940010403
Subject(s) - manduca sexta , midgut , biology , biochemistry , microsome , cytochrome , reductase , enzyme , insect , ecology , botany , larva
The subcellular distribution of four enzymes (glucose‐6‐phosphatase, phosphodiesterase I, NADPH‐cytochrome c reductase, and p ‐nitroanisole O ‐demethylase) in the midgut of “wandering” fifth‐instar larvae of the tobacco hornworm, Manduca sexta (L), was determined and the composition of mitochondrial and microsomal pellets was examined by electron microscopy. Most of the glucose‐6‐phosphatase activity and one‐third of the phosphodiesterase I activity were found in the high‐speed supernatant. NADPH‐cytochrome c reductase activity was marginal and O ‐demethylase activity was undetectable in the supernatant. The highest specific activities for phosphodiesterase I, NADPH‐cytochrome c reductase, and p ‐nitroanisole O ‐demethylase were measured in microsomes, but the relative specific activity of phosphodiesterase I was only half that obtained with the latter two enzymes. In all subcellular preparations the relative specific activities of NADPH‐cytochrome c reductase and p ‐nitroanisole O ‐demethylase were closely correlated. It is concluded that glucose‐6‐phosphatase and phosphodiesterase I are not microsomal marker enzymes in the midgut, but the activities of NADPH‐cytochrome c reductase and p ‐nitroanisole O ‐demethylase are quantitative measures of microsomal content.