Coproheme decarboxylase from Bacillus subtilis is required for bacterial growth and heme b biosynthesis under anaerobic conditions

Heme biosynthesis notably does not follow a universal pathway. Instead, different organisms utilize various routes of producing this essential molecule. The coproporphyrin-dependent (CPD) pathway is unique to Gram-positive bacteria. Given the ubiquity of Gram-positive pathogenic organisms, thorough research on its enzymatic steps is a prerequisite for the development of novel antibiotics. Here the focus lies on coproheme decarboxylase (ChdC, formerly HemQ), the terminal step of the pathway, catalyzing the transformation of Fe-coproporphyrin III (coproheme) to heme b by oxidative decarboxylation. In previous studies, hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) has been shown to act as a necessary co-substrate and electron acceptor for ChdC. However, H<sub>2</sub>O<sub>2</sub>, due to its cytotoxic effects, needs tight intracellular control and is a sub-optimal substrate in vivo, especially during anaerobic growth. To investigate a H<sub>2</sub>O<sub>2</sub>-free pathway for heme biosynthesis, knockout studies on Gram-positive model organism Bacillus subtilis have been performed. These reveal that ΔchdC strains exhibit heme auxotrophic behavior during aerobic and anaerobic growth, highlighting that ChdC has likely no anaerobic alternative. Free and protein bound FMN (in the form of flavodoxins YkuN and YkuP from B. subtilis) were subsequently characterized as alternative co-substrates. Their reaction with heterologously expressed ChdC from B. subtilis was characterized in different settings. By polarographic dioxygen level determination, liquid chromatography, mass spectrometry and time-resolved spectroscopy, these reactions were shown to be possible and promoted under anaerobic conditions and at elevated pH-values. Overall, the results presented in this study confirm the necessity and the capability of ChdC to react anaerobically in a Gram-positive model organism.

Authors

Institutions

Publication Details

Journal
Free Radical Biology and Medicine
Published
2025-08-22
DOI
https://doi.org/10.1016/j.freeradbiomed.2025.08.046
Primary Topic
Porphyrin Metabolism and Disorders
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Coproheme decarboxylase from Bacillus subtilis is required for bacterial growth and heme b biosynthesis under anaerobic conditions

Jörg Stülke, Paul G. Furtmüller, Tim Causon, Stefan Hofbauer et al.
Free Radical Biology and Medicine
Porphyrin Metabolism and Disorders
article

Coproheme decarboxylase from Bacillus subtilis is required for bacterial growth and heme b biosynthesis under anaerobic conditions

Jörg Stülke, Paul G. Furtmüller, Tim Causon, Stefan Hofbauer, Nikolaus Falb, Johannes Stadlmann, Robert Warneke, Nikola Luca Satrapa
article en

Abstract

Heme biosynthesis notably does not follow a universal pathway. Instead, different organisms utilize various routes of producing this essential molecule. The coproporphyrin-dependent (CPD) pathway is unique to Gram-positive bacteria. Given the ubiquity of Gram-positive pathogenic organisms, thorough research on its enzymatic steps is a prerequisite for the development of novel antibiotics. Here the focus lies on coproheme decarboxylase (ChdC, formerly HemQ), the terminal step of the pathway, catalyzing the transformation of Fe-coproporphyrin III (coproheme) to heme b by oxidative decarboxylation. In previous studies, hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) has been shown to act as a necessary co-substrate and electron acceptor for ChdC. However, H<sub>2</sub>O<sub>2</sub>, due to its cytotoxic effects, needs tight intracellular control and is a sub-optimal substrate in vivo, especially during anaerobic growth. To investigate a H<sub>2</sub>O<sub>2</sub>-free pathway for heme biosynthesis, knockout studies on Gram-positive model organism Bacillus subtilis have been performed. These reveal that ΔchdC strains exhibit heme auxotrophic behavior during aerobic and anaerobic growth, highlighting that ChdC has likely no anaerobic alternative. Free and protein bound FMN (in the form of flavodoxins YkuN and YkuP from B. subtilis) were subsequently characterized as alternative co-substrates. Their reaction with heterologously expressed ChdC from B. subtilis was characterized in different settings. By polarographic dioxygen level determination, liquid chromatography, mass spectrometry and time-resolved spectroscopy, these reactions were shown to be possible and promoted under anaerobic conditions and at elevated pH-values. Overall, the results presented in this study confirm the necessity and the capability of ChdC to react anaerobically in a Gram-positive model organism.

Free Radical Biology and MedicineVol. 240
University of Göttingen (DE), BOKU University (AT)
Austrian Science Fund
Zero hunger
Openalex Percentile: Top 81%
Porphyrin Metabolism and Disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.