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Microbial endogenous porphyrins are small-molecule metabolic intermediates produced by many bacteria during the biosynthesis of heme and related compounds. In bacteria such as *Propionibacterium acnes* and *Corynebacterium diphtheriae*, these porphyrins (predominantly coproporphyrin III and protoporphyrin IX) accumulate naturally or after stimulation with precursors such as 5-aminolevulinic acid (ALA)[1][2][3][4][5][6]. Upon exposure to visible light, especially in the blue region, these molecules generate reactive oxygen species, rendering bacteria susceptible to membrane damage and cell death—an effect exploited in photodynamic antimicrobial therapy[1][3][5]. Endogenous porphyrin fluorescence is also used diagnostically to detect certain bacterial infections such as acne[2][4]. These molecules are **not individual, canonical drug targets** like proteins or receptors, but rather functional metabolites with broad roles in microbial physiology, pathogenicity, and medical diagnostics[5][6].
Light activation of accumulated porphyrins generates reactive oxygen species (e.g., singlet oxygen), causing bacterial cell damage and death through membrane disruption and oxidative injury
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