Melissa K Gómez Ríos

Dr. Melissa K Gómez Ríos

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Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 March 2019 in Frontiers in Microbiology
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MGMaría Soledad Gutiérrez
María Soledad Gutiérrez
SCSebastián Campusano
Sebastián Campusano
AGAna María González
Ana María González
MRMelissa K Gómez Ríos
Melissa K Gómez Ríos
SBSalvador Barahona
Salvador Barahona
JAJennifer Alcaino
Jennifer Alcaino
Xanthophyllomyces dendrorhous is a basidiomycete yeast that synthesizes carotenoids, mainly astaxanthin, which are of great commercial interest. Currently, there are many unknown aspects related to regulatory mechanisms on the synthesis of carotenoids in this yeast. Our recent studies showed that changes in sterol levels and composition resulted in upregulation of genes in the mevalonate pathway required for the synthesis of carotenoid precursors, leading to increased production of these pigments. Sterol Regulatory Element-Binding Proteins (SREBP), called Sre1 in yeast, are conserved transcriptional regulators of sterol homeostasis and other cellular processes. Given the results linking sterols and carotenoids, we investigated the role of SREBP in sterol and carotenoid synthesis in X. dendrorhous. In this study, we present the identification and functional characterization of the X. dendrorhous SRE1 gene, which encodes the transcription factor Sre1. The deduced protein has the characteristic features of SREBP/Sre1 and binds to consensus DNA sequences in vitro. RNA-seq analysis and chromatin-immunoprecipitation experiments showed that genes of the mevalonate pathway and ergosterol biosynthesis are directly regulated by Sre1. The sre1- mutation reduced sterol and carotenoid production in X. dendrorhous, and expression of the Sre1 N-terminal domain (Sre1N) increased carotenoid production more than twofold compared to wild-type. Overall, our results indicate that in X. dendrorhous transcriptional regulation of genes in the mevalonate pathway control production of the isoprenoid derivatives, carotenoids and sterol. Our results provide new insights into the conserved regulatory functions of SREBP/Sre1 and identify pointing to the SREBP pathway as a potential target to enhance carotenoid production in X. dendrorhous.

1 December 2020 in Journal of Lipid Research
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MRMelissa K Gómez Ríos
Melissa K Gómez Ríos
SCSebastián Campusano
Sebastián Campusano
MGMaría Soledad Gutiérrez
María Soledad Gutiérrez
DSDionisia Sepúlveda
Dionisia Sepúlveda
SBSalvador Barahona
Salvador Barahona
JAJennifer Alcaino
Jennifer Alcaino
Melissa Gómez, Sebastián Campusano, María Soledad Gutiérrez, Dionisia Sepúlveda, Salvador Barahona, Marcelo Baeza, Victor Cifuentes, Jennifer Alcaíno

26 October 2021 in Biological Research
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MRMelissa K Gómez Ríos
Melissa K Gómez Ríos
MBMarcelo Baeza
Marcelo Baeza
VCVíctor Cifuentes
Víctor Cifuentes
JAJennifer Alcaino
Jennifer Alcaino
Xanthophyllomyces dendrorhous is a basidiomycete yeast that naturally produces the red–orange carotenoid astaxanthin, which has remarkable antioxidant properties. The biosynthesis of carotenoids and sterols share some common elements that have been studied in X. dendrorhous. For example, their synthesis requires metabolites derived from the mevalonate pathway and in both specific pathways, cytochrome P450 enzymes are involved that share a single cytochrome P450 reductase, CrtR, which is essential for astaxanthin biosynthesis, but is replaceable for ergosterol biosynthesis. Research on the regulation of carotenoid biosynthesis is still limited in X. dendrorhous; however, it is known that the Sterol Regulatory Element-Binding Protein (SREBP) pathway, which is a conserved regulatory pathway involved in the control of lipid metabolism, also regulates carotenoid production in X. dendrorhous. This review addresses the similarities and differences that have been observed between mammal and fungal SREBP pathways and what it is known about this pathway regarding the regulation of the production of carotenoids and sterols in X. dendrorhous.

1 February 2020 in Journal of Lipid Research
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MRMelissa K Gómez Ríos
Melissa K Gómez Ríos
MGMaría Soledad Gutiérrez
María Soledad Gutiérrez
AGAna María González
Ana María González
CGCarla Gárate-Castro
Carla Gárate-Castro
DSDionisia Sepúlveda
Dionisia Sepúlveda
JAJennifer Alcaino
Jennifer Alcaino
Melissa Gómez, María Soledad Gutiérrez, Ana María González, Carla Gárate-Castro, Dionisia Sepúlveda, Salvador Barahona, Marcelo Baeza, Victor Cifuentes, Jennifer Alcaíno

21 November 2016 in BMC Microbiology
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NWNicole Werner
Nicole Werner
MRMelissa K Gómez Ríos
Melissa K Gómez Ríos
MBMarcelo Baeza
Marcelo Baeza
VCVíctor Cifuentes
Víctor Cifuentes
JAJennifer Alcaino
Jennifer Alcaino
The basidiomycetous yeast Xanthophyllomyces dendrorhous has been described as a potential biofactory for terpenoid-derived compounds due to its ability to synthesize astaxanthin. Functional knowledge of the genes involved in terpenoid synthesis would create opportunities to enhance carotenoid production. A thiolase enzyme catalyzes the first step in terpenoid synthesis. Two potential thiolase-encoding genes were found in the yeast genome; bioinformatically, one was identified as an acetyl-CoA C-acetyltransferase (ERG10), and the other was identified as a 3-ketoacyl Co-A thiolase (POT1). Heterologous complementation assays in Saccharomyces cerevisiae showed that the ERG10 gene from X. dendrorhous could complement the lack of the endogenous ERG10 gene in S. cerevisiae, thereby allowing cellular growth and sterol synthesis. X. dendrorhous heterozygous mutants for each gene were created, and a homozygous POT1 mutant was also obtained. This mutant exhibited changes in pigment composition and higher ERG10 transcript levels than the wild type strain. The results support the notion that the ERG10 gene in X. dendrorhous is a functional acetyl-CoA C-acetyltransferase essential for the synthesis of mevalonate in yeast. The POT1 gene would encode a functional 3-ketoacyl Co-A thiolase that is non-essential for cell growth, but its mutation indirectly affects pigment production.

2 February 2022 in Journal of Lipid Research
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Journal Article
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AGAna-María González
Ana-María González
MVMaximiliano Venegas
Maximiliano Venegas
SBSalvador Barahona
Salvador Barahona
MRMelissa K Gómez Ríos
Melissa K Gómez Ríos
MGMaría-Soledad Gutiérrez
María-Soledad Gutiérrez
JAJennifer Alcaino
Jennifer Alcaino
Cytochrome P450s (P450s) are heme-containing proteins involved in several cellular functions, including biosynthesis of steroidal hormones, detoxification of xenobiotic compounds, among others. Damage response protein 1 (Dap1) has been described as a positive regulator of P450s through protein-protein interactions in organisms such as Schizosaccharomyces pombe. Three P450s in the carotenogenic yeast Xanthophyllomyces dendrorhous have thus far been characterized: Cyp51 and Cyp61, which are involved in ergosterol biosynthesis, and CrtS (astaxanthin synthase), which is involved in biosynthesis of the carotenoid astaxanthin. In this work, we describe the X. dendrorhous DAP1 gene, deletion of which affected yeast pigmentation by decreasing the astaxanthin fraction and increasing the β-carotene (a substrate of CrtS) fraction, which is consistent with the known role of CrtS. We found that the proportion of ergosterol was also decreased in the Δdap1 mutant. However, even though the fractions of the end products of these two pathways (the synthesis of carotenoids and sterols) were decreased in the Δdap1 mutant, the transcript levels of genes from the P450 systems involved were higher than those in the wild-type strain. We demonstrate that Dap1 coimmunoprecipitates with these three P450s, suggesting that Dap1 interacts with these three proteins. We propose that Dap1 regulates the synthesis of astaxanthin and ergosterol in X. dendrorhous, probably by regulating the P450s involved in both biosynthetic pathways at the protein level. This work suggests a new role for Dap1 in the regulation of carotenoid biosynthesis in X. dendrorhous.