| Autor: |
Jiang H; Department of Biochemistry, Kansas State University, Manhattan 66506, USA., Wang Y, Korochkina SE, Benes H, Kanost MR |
| Jazyk: |
angličtina |
| Zdroj: |
Insect biochemistry and molecular biology [Insect Biochem Mol Biol] 1997 Jul; Vol. 27 (7), pp. 693-9. |
| DOI: |
10.1016/s0965-1748(97)00045-3 |
| Abstrakt: |
Phenol oxidase exists in insect hemolymph as a zymogen, pro-phenol oxidase (pro-PO), which is activated by specific proteolysis in response to infection or wounding. Phenol oxidase catalyses the synthesis of quinones that polymerize to form melanin deposits, which encapsulate parasites and help to seal wounds. Antibodies to pro-PO from Manduca sexta bound to 76, 72, and 71 kDa polypeptide bands from hemolymph of Anopheles gambiae larvae. This antiserum was used to screen a cDNA library from A. gambiae fourth-instar larvae. Full-length clones were isolated for two different pro-POs, designated A. gambiae proPO-p1 and proPO-p2, which are 67% identical in nucleotide sequence and 66% identical in deduced amino acid sequence. The A. gambiae pro-PO sequences are more similar to pro-PO from Drosophila melanogaster than to lepidopteran or crustacean pro-PO sequences in the GenBank database. Like the other arthropod pro-POs, the A. gambiae pro-PO sequences lack a signal peptide and have two conserved regions predicted to bind two copper atoms in the active site of the enzyme. The availability of these pro-PO cDNAs should be useful in examining the biochemical differences between A. gambiae strains that are refractory or susceptible to Plasmodium infection, and differ in their ability to encapsulate the parasites. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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