Mechanisms of the marine yeast <i>Debaryomyces hansenii</i> for protection against reactive oxygen species produced during benzo(a)pyrene biotransformation

Polycyclic aromatic hydrocarbons (PAHs), such as benzo(a)pyrene (BaP), are persistent environmental pollutants recognized for their high toxicity and resistance to microbial degradation. The marine yeast <i>Debaryomyces hansenii</i> has emerged as a compelling candidate due to its ability to thrive under a variety of stressful conditions. This study presents a molecular and biochemical analysis of the responses of <i>D. hansenii</i> to BaP exposure, providing insights into the detoxification and antioxidant mechanisms. In this study, we explored BaP removal from the medium and characterized the associated molecular and biochemical responses induced by this compound. Our findings demonstrate that <i>D. hansenii</i> can grow in BaP concentrations up to 100 ppm without compromising cell viability and is capable of biotransforming nearly 70% of the compound within 6 days. This process involved cytochrome P450 (CYP), epoxide hydrolase (EH), and glutathione S-transferase (GST), enzymes typically associated with xenobiotic metabolism. BaP exposure resulted in pronounced oxidative stress, evidenced by elevated ROS levels, lipid peroxidation, and protein carbonylation. However, <i>D. hansenii</i> activated a robust antioxidant defense, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and regulation of the glutathione redox system. Altogether, these results show that <i>D. hansenii</i> maintains redox homeostasis during BaP biotransformation through a coordinated enzymatic network that links xenobiotic metabolism with antioxidant protection, thereby expanding mechanistic understanding and providing a basis for future studies under environmentally relevant conditions.IMPORTANCEUnderstanding how marine yeasts respond to polycyclic aromatic hydrocarbons (PAHs) is important for advancing our knowledge of stress adaptation and xenobiotic biotransformation in extremophilic microorganisms. <i>Debaryomyces hansenii</i> is a suitable model organism because it naturally tolerates high salinity, oxidative conditions, and nutrient limitation. By characterizing its responses to benzo(a)pyrene (BaP), we can gain insight into how eukaryotic microbes activate biotransformation pathways and antioxidant defenses under chemical stress. This insight contributes to a broader comprehension of cellular strategies for coping with toxic contaminants and provides the basis for future applied research.

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Publication Details

Journal
Applied and Environmental Microbiology
Published
2026-01-07
DOI
https://doi.org/10.1128/aem.02314-25
Citations
1
Primary Topic
Microbial bioremediation and biosurfactants
Type
article
Field-Weighted Citation Impact
18.32
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article

Mechanisms of the marine yeast Debaryomyces hansenii for protection against reactive oxygen species produced during benzo(a)pyrene biotransformation

Antonio Peña, Minerva Georgina Araiza-Villanueva, Martha Calahorra, Francisco Padilla-Garfias et al.
1 citations
Applied and Environmental Microbiology
Microbial bioremediation and biosurfactants
18.32
article

Mechanisms of the marine yeast Debaryomyces hansenii for protection against reactive oxygen species produced during benzo(a)pyrene biotransformation

Antonio Peña, Minerva Georgina Araiza-Villanueva, Martha Calahorra, Francisco Padilla-Garfias, Norma Silvia Sánchez
article en
1 citations

Abstract

Polycyclic aromatic hydrocarbons (PAHs), such as benzo(a)pyrene (BaP), are persistent environmental pollutants recognized for their high toxicity and resistance to microbial degradation. The marine yeast <i>Debaryomyces hansenii</i> has emerged as a compelling candidate due to its ability to thrive under a variety of stressful conditions. This study presents a molecular and biochemical analysis of the responses of <i>D. hansenii</i> to BaP exposure, providing insights into the detoxification and antioxidant mechanisms. In this study, we explored BaP removal from the medium and characterized the associated molecular and biochemical responses induced by this compound. Our findings demonstrate that <i>D. hansenii</i> can grow in BaP concentrations up to 100 ppm without compromising cell viability and is capable of biotransforming nearly 70% of the compound within 6 days. This process involved cytochrome P450 (CYP), epoxide hydrolase (EH), and glutathione S-transferase (GST), enzymes typically associated with xenobiotic metabolism. BaP exposure resulted in pronounced oxidative stress, evidenced by elevated ROS levels, lipid peroxidation, and protein carbonylation. However, <i>D. hansenii</i> activated a robust antioxidant defense, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and regulation of the glutathione redox system. Altogether, these results show that <i>D. hansenii</i> maintains redox homeostasis during BaP biotransformation through a coordinated enzymatic network that links xenobiotic metabolism with antioxidant protection, thereby expanding mechanistic understanding and providing a basis for future studies under environmentally relevant conditions.IMPORTANCEUnderstanding how marine yeasts respond to polycyclic aromatic hydrocarbons (PAHs) is important for advancing our knowledge of stress adaptation and xenobiotic biotransformation in extremophilic microorganisms. <i>Debaryomyces hansenii</i> is a suitable model organism because it naturally tolerates high salinity, oxidative conditions, and nutrient limitation. By characterizing its responses to benzo(a)pyrene (BaP), we can gain insight into how eukaryotic microbes activate biotransformation pathways and antioxidant defenses under chemical stress. This insight contributes to a broader comprehension of cellular strategies for coping with toxic contaminants and provides the basis for future applied research.

Applied and Environmental MicrobiologyVol. 92(2)
Universidad Nacional Autónoma de México (MX)
Life below water
Openalex Percentile: Top 4%
Microbial bioremediation and biosurfactants
18.32
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