INVESTIGADORES
CARRILLO carolina
congresos y reuniones científicas
Título:
HPLC separation and analysis method to evaluate molecules involved in the arginine-ornithine cycle in Phytomonas
Autor/es:
FRACCAROLI L; TORRES P; RUIZ MD; MARCORA MS; DE PINO V; CARRILLO C
Lugar:
Ciudad autonoma de Buenos Aires
Reunión:
Congreso; Reunión Conjunta de Sociedades de Biociencia 2017; 2017
Institución organizadora:
Sociedades Científicas Argentinas
Resumen:
Phytomonas spp. are trypanosomatid parasites that infect a variety of plants andcan cause diseases that affect regional economies, mainly in South America. Little is known about Phytomonas biology; however, recently published genomic data provide new venues for research. We are interested in the study of arginine ? ornithine cycle with special focus on the enzymes involved in the conversion of arginine-citrulline-ornithine.To confirm our previous evidences about the presence of NOS and ODC and theabsence of ADC and AGMATINASE enzymes in this cycle, we set up a method forseparation and analysis of products and intermediates using high-performanceliquid chromatography (HPLC) that involves precolumn derivatization witho-phthaldialdehyde, C18 analytical column and fluorescence detection. We testedtwo mobile phase solutions (MP): 1- MPA: 0.1M sodium acetate, pH7.2/MPB:100% methanol and 2- MPA: 25mM phosphate buffer pH7.5/MPB:acetonitrile:methanol:water 45:45:10, both at three different temperatures (15, 25 and 40oC). Under these different conditions we separated a mixture of standard aminoacids: arginine, ornithine, citrulline, agmatine, lysine, glycine and threonine.We found that mobile phase 2 at 40oC was the best condition to obtain individualpeaks for each aminoacid with a detection limit of at least 1uM. As a first in vivo approach, Phytomonas Jma was cultured in a semi-defined media (SDM-79) andextracts obtained from 2 and 10x106 cells were deproteinized and neutralized. The HPLC chromatogram, under the selected conditions, showed the seven aminoacidpeaks well resolved and a low background signal. Further analysis will be made to analyze the aminoacid profile under different culture conditions.In conclusion, we have set up a HPLC protocol that will be useful to analyzePhytomonas metabolism. This method could also be used to analyze aminoacidsin a variety of biological samples such as physiological fluids, tissue extracts and different cell types.