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Candida glabrata tryptophan‐based pigment production via the Ehrlich pathway
Author(s) -
Brunke Sascha,
Seider Katja,
Almeida Ricardo Sergio,
Heyken Antje,
Fleck Christian Benjamin,
Brock Matthias,
Barz Dagmar,
Rupp Steffen,
Hube Bernhard
Publication year - 2010
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2010.07052.x
Subject(s) - biology , pigment , mutant , tryptophan , candida glabrata , biochemistry , yeast , microbiology and biotechnology , gene , amino acid , antifungal , chemistry , organic chemistry
Summary Pigments contribute to the pathogenicity of many fungi, mainly by protecting fungal cells from host defence activities. Here, we have dissected the biosynthetic pathway of a tryptophan‐derived pigment of the human pathogen Candida glabrata , identified key genes involved in pigment production and have begun to elucidate the possible biological function of the pigment. Using transcriptional analyses and a transposon insertion library, we have identified genes associated with pigment production. Targeted deletion mutants revealed that the pigment is a by‐product of the Ehrlich pathway of tryptophan degradation: a mutant lacking a tryptophan‐upregulated aromatic aminotransferase (Aro8) displayed significantly reduced pigmentation and a recombinantly expressed version of this protein was sufficient for pigment production in vitro . Pigment production is tightly regulated as the synthesis is affected by the presence of alternative nitrogen sources, carbon sources, cyclic AMP and oxygen. Growth of C. glabrata on pigment inducing medium leads to an increased resistance to hydrogen peroxide, an effect which was not observed with a mutant defective in pigmentation. Furthermore, pigmented yeast cells had a higher survival rate when exposed to human neutrophils and caused increased damage in a monolayer model of human epithelia, indicating a possible role of pigmentation during interactions with host cells.