Efeitos do estresse biótico na expressão de terpenos em plantas: Varronia curassavica Jacq. and Pistacia palaestina Boiss

Abstract

Terpenes are a large and diverse class of natural products, being associated with plant metabolism and interactions with other organisms. Nowadays compounds and enzymes of the terpenes pathway in plants are widely studied in different aspects. Varronia curassavica and Pistacia palaestina were the selected species to study the biotic stress effects on terpenoids expressions. Leaves of V. curassavica are the commercial source α-humulene and β-caryophyllene, sesquiterpenes with anti-inflammatory properties. The objective of this study was to evaluate the effect of two natural elicitors on the sesquiterpene content of V. curassavica. Thus, field grown plants received the application of acibenzolar-S-methyl (500 mg L-1), 1,6 -D-glucan obtained from Lasiodiplodia theobromae (50 mg L-1) and distilled water as a control. Gas exchange rate, terpene enzymes such as phenylalanine ammonia-lyase, superoxide dismutase, guaiacol peroxidase and catalase activity and essential oil content in leaves were measured. Acibenzolar-S-methyl reduced significantly the net carbon assimilation rate and the intercellular CO2 concentration, while1,6 -D-glucan reduced significantly only the intercellular CO2 concentration. The highest essential oil yield (0.819%) was obtained in plants elicited with 1,6 -D-glucan. The content of α-humulene and β-caryophyllene did not differ among treatments however the elicitors provided a significant increase in guaiacol peroxidase activity. Terpenes are present in Pistacia palaestina in leaves and in horn-shaped galls. The mechanism of gall development remains unknown, however it is clear Baizongia pistaciae L., an aphid species, manipulates their hosts anatomy, physiology, and chemistry for their own benefit. To isolate and functional characterize terpene synthase genes from galls induced by B. pistaciae as well as their gene relative expression by RT-qPCR in leaves and galls of P. palestina were the aims of this study. The heterologous expression was performed in E. coli pLYS-BL21 cells, being enzymatic assay reactions made with the purified proteins using geranyl diphosphate (GPP) or farnesyl diphosphate (FPP) to test for possible mono- and sesquiterpene synthase activity, respectively. For relative real-time PCR, it was selected an appropriate reference gene between actin, cyclophilin, phosphoglycerate kinase, RNA polymerase II, α-tubulin and ubiquitin. After selection, it was performed reactions with terpene synthases genes to evaluate differences in expression levels in P. palaestina non-colonized leaves and galls. Two monoterpene synthases (PpTPS281 and PpTPS809) and one sesquiterpene synthase (PpTPS232) were isolated and characterized in P. palaestina. PpTPS281 produced exclusively D-limonene from GPP, while PpTPS809 produced several monoterpenes from GPP and PpTPS232 catalyzed the formation of different sesquiterpenes from FPP. Real-time PCR results showed that actin is the most proper gene to be used for genes expression studies between non-colonized P. palaestina leaves and galls induced by B. pistaciae. The levels of expression of the genes were significantly upregulated in galls (from 2,21- to 96.5-fold) when compared to leaves.