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A pH-dependent direct sulfhydrylation pathway is required for the pathogenesis of Mycobacterium tuberculosis - Communications Biology
Abstract Methionine is essential for the growth and survival of Mycobacterium tuberculosis (M. tuberculosis), however, the canonical transsulfuration pathway involved in the biosynthesis of methionine is dispensable, suggesting redundancy. This study explores the presence of an ortholog of O-succinyl homoserine sulfhydrylase in M. tuberculosis, which catalyses direct sulfhydrylation for methionine biosynthesis.
pH dependent direct sulfhydrylation pathway is required for the pathogenesis of Mycobacterium tuberculosis
Abstract Methionine is essential for the survival of Mycobacterium tuberculosis (M. tuberculosis) inside the host. However, the transsulfuration pathway, a major contributor of methionine, is dispensable for the growth of M. tuberculosis suggesting redundancy in the methionine biosynthesis pathway. Orthologues of MetZTB in other bacterial species are known to operate a redundant single-step methionine biosynthesis pathway called direct sulfhydrylation.
pH dependent direct sulfhydrylation pathway is required for pathogenesis of Mycobacterium tuberculosis
Abstract Methionine is essential for the survival of Mycobacterium tuberculosis (M. tuberculosis) inside the host. Inhibiting the transsulfuration pathway fails to exhibit methionine auxotrophy suggesting the presence of an alternate methionine biosynthesis pathway in M. tuberculosis. Orthologues of MetZTB in other bacterial species are known to regulate a redundant single step methionine biosynthesis pathway known as direct sulfhydrylation.
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