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Mai, B.-X.

Publications and source records attributed to Mai, B.-X..

2 recordsLinked to original sources

Light-dependent and predator inducible aldehyde synthesis in Prochlorococcus for specific defense against Uronema

Cyanobacteria as a primary producer provide energy and carbon sources for the marine food web, of which predation-interactions play central roles in regulating global element cycles and marine ecosystem stability. Here, we report the anti-predation activity of a typical marine cyanobacterium Prochlorococcus MED4 to defend the predation by Uronema marinum. MED4 synthesize formaldehyde as the anti-predation chemical, of which the synthesis was light-dependent and predator-inducible. Compared to other protists, both the higher concentration of accumulated formaldehyde in U. marinum and the lower formaldehyde tolerance of U. marinum resulted in the specific anti-predation of MED4 against U. marinum. This specific anti-predation could regulate the cyanobacterial growth and the U. marinum infection of marine fishes. Metadata analyses showed the mutually exclusion of Prochlorococcus and Uronema in global marine environments. These findings significantly advance our understanding of the marine food web and biogeochemical cycles. Significance StatementPredation-driven interactions in the ocean are critical regulators of global biogeochemical cycles, yet active defense mechanisms in marine picophytoplankton remain largely unknown. This study reveals that Prochlorococcus MED4 as the most abundant primary producer in the ocean synthesize light-driven and predator-inducible aldehydes to actively and specifically defend predation against the ciliate Uronema marinum. The anti-predation of Prochlorococcus against Uronema could have broad implications in biocontrol of Uronema infection in marine fishes and regulation of the marine food web.

microbiology↗

Metabolic dehalogenation of halomethanes by mercury methylators

Mercury (Hg) methylators play key roles in the global Hg cycle. Nonetheless, the Hg methylators are widely present in Hg-absent environments and the Hg methylation is a cometabolic process without cell growth, which leave the origin and evolution of the Hg methylation as a mystery. Here, we reported the CCl4/trihalomethane-to-dihalomethane dehalogenation by model Hg methylators in a metabolic way. Heterologously-expressed HgcAB catalyzed both the CCl4 dechlorination and Hg methylation. Halomethanes were shown to sustain the Hg-methylation community without adding external carbon source, electron donor and acceptor. Metadata analyses suggested the halomethane dehalogenation potential of Hg methylators at the global scale. These results, together with much higher global flux and kinetic Vmax of the metabolic halomethanes dehalogenation relative to the co-metabolic Hg methylation, suggested halomethanes as the potential HgcAB substrates for the evolution of Hg methylation.

microbiology↗