Key result
Cloning and expression of NOS cDNA from Rhodnius prolixus salivary glands revealed a 132 kDa Ca2+/calmodulin-dependent soluble enzyme lacking a large N-terminal domain and myristylation sequence.
The study successfully cloned and characterized a unique nitric-oxide synthase from the salivary glands of Rhodnius prolixus, demonstrating its structural and functional similarities and differences compared to mammalian NOS isoforms.
No immediate clinical implications; leaves open whether this insect NOS variant informs mammalian isoform-specific cardiovascular research.
Rhodnius prolixus, a blood-sucking bug, is a unique insect that is known to produce nitric oxide (NO) in the salivary glands to use as a vasodilator for blood sucking. We report here the cloning of the NO synthase (NOS) cDNA from these salivary glands and its expression in a baculovirus system. This cDNA encodes a protein of 1174 amino acids with a calculated molecular mass of 132,331 Da. The primary structures of mammalian NOS, including the putative cofactor-recognition sites for heme, tetrahydrobiopterin (BH4), calmodulin. FMN, FAD and NADPH are all conserved in salivary-gland NOS. Recombinant salivary-gland NOS differed from nerve NOS and endothelial NOS in that it lacked a large N-terminal domain and an N-terminal myristylation sequence, respectively. Salivary-gland NOS produced in a baculovirus system showed NOS activity and demonstrated that salivary-gland NOS was soluble and was Ca2+ and calmodulin dependent, similarly to mammalian constitutive NOS isoforms. Recombinant salivary-gland NOS was purified to near homogeneity and migrated at 130 kDa on SDS/PAGE.
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Yuda et al. (1996) studied this question. cDNA cloning and expression of NOS was evaluated on Characterization of salivary-gland NOS. Cloning and expression of NOS cDNA from Rhodnius prolixus salivary glands revealed a 132 kDa Ca2+/calmodulin-dependent soluble enzyme lacking a large N-terminal domain and myristylation sequence.
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