dc.creatorRossi, Guilherme D.
dc.creatorLabate, Monica T. V.
dc.creatorLabate, Carlos A.
dc.creatorVinson, S. B.
dc.creatorConsoli, Fernando L.
dc.date.accessioned2013-09-13T17:59:37Z
dc.date.accessioned2018-07-04T15:55:56Z
dc.date.available2013-09-13T17:59:37Z
dc.date.available2018-07-04T15:55:56Z
dc.date.created2013-09-13T17:59:37Z
dc.date.issued2012
dc.identifierPESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, SAN DIEGO, v. 104, n. 2, Special Issue, pp. 96-102, OCT, 2012
dc.identifier0048-3575
dc.identifierhttp://www.producao.usp.br/handle/BDPI/33350
dc.identifier10.1016/j.pestbp.2012.07.005
dc.identifierhttp://dx.doi.org/10.1016/j.pestbp.2012.07.005
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1629346
dc.description.abstractThe larval endoparasitoid Toxoneuron nigriceps (Viereck) (Hymenoptera: Braconidae) has a toolbox of biological weapons to secure for host colonization and the successful parasitization of its host Heliothis virescens (F.) (Lepidoptera: Noctuidae). The cDNA of a putative chitinase has been previously isolated and initially characterized from teratocytes of this parasitoid among the plethora of molecules available in the venom and calyx fluids injected by females, oral and/or anal secretions released by the parasitoid larvae and/or produced by the expression of genes of the symbiotic associated polydnavirus. This putative chitinase has been initially associated with the host cuticle digestion to allow for parasitoid egression and with the asepsis of the host environment, acting as an antimicrobial. As chitinases are commonly expressed in plants against plant pathogens, the chitinase derived from the teratocytes of T. nigriceps is a potential tool for the development of insect pest control methods based on the disruption of the perithrophic membrane of herbivores. Therefore, we aimed to characterize the activity of the putative chitinase from teratocytes of T. nigriceps (Tnchi) produced using the Escherichia coli expression system and its potential to control H. virescens larvae when expressed into transgenic tobacco plants. The purified E. coli-produced Tnchi protein showed no chitinolitic activity, but was active in binding with colloidal and crystalline chitins in water and with colloidal chitin in buffered solution (pH = 6.74). Transgenic tobacco plants showed no enhanced chitinolitic activity relative to control plants, but survival of three-day old larvae of H. virescens was severely affected when directly fed on transgenic tobacco leaves expressing the recombinant Tnchi protein. Some properties of the Tnchi protein and the potential use of Tnchi-transgenic plants to control plant pests are discussed. (c) 2012 Elsevier Inc. All rights reserved.
dc.languageeng
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE
dc.publisherSAN DIEGO
dc.relationPESTICIDE BIOCHEMISTRY AND PHYSIOLOGY
dc.rightsCopyright ACADEMIC PRESS INC ELSEVIER SCIENCE
dc.rightsclosedAccess
dc.subjectBIOTECHNOLOGY
dc.subjectCHITOLECTINS
dc.subjectCHITOTRIOSIDASES
dc.subjectPARASITOID
dc.subjectTERATOCYTES
dc.titleCharacterization of a Toxoneuron nigriceps (Viereck) (Hymenoptera: Braconidae) - derived chitinase and its potential for pest control
dc.typeArtículos de revistas


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