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1.
Microbiology (Reading) ; 163(3): 343-354, 2017 03.
Artículo en Inglés | MEDLINE | ID: mdl-28073401

RESUMEN

Rhodococcus jostii RHA1 is able to degrade toxic compounds and accumulate high amounts of triacylglycerols (TAG) upon nitrogen starvation. These NADPH-dependent processes are essential for the adaptation of rhodococci to fluctuating environmental conditions. In this study, we used an MS-based, label-free and quantitative proteomic approach to better understand the integral response of R. jostii RHA1 to the presence of methyl viologen (MV) in relation to the synthesis and accumulation of TAG. The addition of MV promoted a decrease of TAG accumulation in comparison to cells cultivated under nitrogen-limiting conditions in the absence of this pro-oxidant. Proteomic analyses revealed that the abundance of key proteins of fatty acid biosynthesis, the Kennedy pathway, glyceroneogenesis and methylmalonyl-CoA pathway, among others, decreased in the presence of MV. In contrast, some proteins involved in lipolysis and ß-oxidation of fatty acids were upregulated. Some metabolic pathways linked to the synthesis of NADPH remained activated during oxidative stress as well as under nitrogen starvation conditions. Additionally, exposure to MV resulted in the activation of complete antioxidant machinery comprising superoxide dismutases, catalases, mycothiol biosynthesis, mycothione reductase and alkyl hydroperoxide reductases, among others. Our study suggests that oxidative stress response affects TAG accumulation under nitrogen-limiting conditions through programmed molecular mechanisms when both stresses occur simultaneously.


Asunto(s)
Nitrógeno/deficiencia , Estrés Oxidativo/fisiología , Paraquat/metabolismo , Rhodococcus/metabolismo , Triglicéridos/biosíntesis , Acilcoenzima A/metabolismo , Adaptación Fisiológica , Catalasa/metabolismo , Cisteína/biosíntesis , Ácidos Grasos/biosíntesis , Glicopéptidos/biosíntesis , Inositol/biosíntesis , NADP/metabolismo , Nitrógeno/metabolismo , Oxidación-Reducción/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Oxidorreductasas/biosíntesis , Peroxirredoxinas/biosíntesis , Proteoma , Rhodococcus/crecimiento & desarrollo , Superóxido Dismutasa/metabolismo
2.
Microbiology (Reading) ; 161(Pt 3): 593-610, 2015 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-25564499

RESUMEN

The bacterium Rhodococcus jostii RHA1 synthesizes large amounts of triacylglycerols (TAGs) under conditions of nitrogen starvation. To better understand the molecular mechanisms behind this process, we performed proteomic studies in this oleaginous bacterium. Upon nitrogen starvation, we observed a re-routing of the carbon flux towards the formation of TAGs. Under these conditions, the cellular lipid content made up more than half of the cell's dry weight. On the proteome level, this coincided with a shift towards non-glycolytic carbohydrate-metabolizing pathways. These pathways (Entner-Doudoroff and pentose-phosphate shunt) contribute NADPH and precursors of glycerol 3-phosphate and acetyl-CoA to lipogenesis. The expression of proteins involved in the degradation of branched-chain amino acids and the methylmalonyl-CoA pathway probably provided propionyl-CoA for the biosynthesis of odd-numbered fatty acids, which make up almost 30 % of RHA1 fatty acid composition. Additionally, lipolytic and glycerol-degrading enzymes increased in abundance, suggesting a dynamic cycling of cellular lipids. Conversely, abundance of proteins involved in consuming intermediates of lipogenesis decreased. Furthermore, we identified another level of lipogenesis regulation through redox-mediated thiol modification in R. jostii. Enzymes affected included acetyl-CoA carboxylase and a ß-ketoacyl-[acyl-carrier protein] synthase II (FabF). An integrative metabolic model for the oleaginous RHA1 strain is proposed on the basis of our results.


Asunto(s)
Proteínas Bacterianas/metabolismo , Rhodococcus/metabolismo , Triglicéridos/metabolismo , Proteínas Bacterianas/química , Proteínas Bacterianas/genética , Ácidos Grasos/metabolismo , Oxidación-Reducción , Proteómica , Rhodococcus/química , Rhodococcus/genética
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