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. 2016 Aug 15;82(17):5077-88.
doi: 10.1128/AEM.00203-16. Print 2016 Sep 1.

Differential Regulation of the Two Ferrochelatase Paralogues in Shewanella loihica PV-4 in Response to Environmental Stresses

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Differential Regulation of the Two Ferrochelatase Paralogues in Shewanella loihica PV-4 in Response to Environmental Stresses

Dongru Qiu et al. Appl Environ Microbiol. .

Abstract

Determining the function and regulation of paralogues is important in understanding microbial functional genomics and environmental adaptation. Heme homeostasis is crucial for the survival of environmental microorganisms. Most Shewanella species encode two paralogues of ferrochelatase, the terminal enzyme in the heme biosynthesis pathway. The function and transcriptional regulation of two ferrochelatase genes, hemH1 and hemH2, were investigated in Shewanella loihica PV-4. The disruption of hemH1 but not hemH2 resulted in a significant accumulation of extracellular protoporphyrin IX (PPIX), the precursor to heme, and decreased intracellular heme levels. hemH1 was constitutively expressed, and the expression of hemH2 increased when hemH1 was disrupted. The transcription of hemH1 was regulated by the housekeeping sigma factor RpoD and potentially regulated by OxyR, while hemH2 appeared to be regulated by the oxidative stress-associated sigma factor RpoE2. When an oxidative stress condition was mimicked by adding H2O2 to the medium or exposing the culture to light, PPIX accumulation was suppressed in the ΔhemH1 mutant. Consistently, transcriptome analysis indicated enhanced iron uptake and suppressed heme synthesis in the ΔhemH1 mutant. These data indicate that the two paralogues are functional in the heme synthesis pathway but regulated by environmental conditions, providing insights into the understanding of bacterial response to environmental stresses and a great potential to commercially produce porphyrin compounds.

Importance: Shewanella is capable of utilizing a variety of electron acceptors for anaerobic respiration because of the existence of multiple c-type cytochromes in which heme is an essential component. The cytochrome-mediated electron transfer across cellular membranes could potentially be used for biotechnological purposes, such as electricity generation in microbial fuel cells and dye decolorization. However, the mechanism underlying the regulation of biosynthesis of heme and cytochromes is poorly understood. Our study has demonstrated that two ferrochelatase genes involved in heme biosynthesis are differentially regulated in response to environmental stresses, including light and reactive oxygen species. This is an excellent example showing how bacteria have evolved to maintain cellular heme homeostasis. More interestingly, the high yields of extracellular protoporphyrin IX by the Shewanella loihica PV-4 mutants could be utilized for commercial production of this valuable chemical via bacterial fermentation.

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Figures

FIG 1
FIG 1
Effects of hemH1 disruption and deletion on phenotypes in PV-4. Inactivation of a ferrochelatase gene resulted in the overproduction of protoporphyrin IX in Shewanella loihica PV-4. The transposon insertional mutant (hemH1::Kmr) and in-frame deletion mutant (PV-4 ΔhemH1) exhibited similar phenotypes, while the deletion of another paralog, hemH2, did not cause the same phenotypes. In genetic complementation analyses on the hemH1 deletion mutant PV-4 ΔhemH1, the plasmid-borne wild-type hemH1 gene restored the phenotype of the mutant to that of the wild-type strain carrying the empty vector.
FIG 2
FIG 2
Chemical analyses of the extracellular compound. (a) Comparison of high-performance liquid chromatography-mass spectrometry extract ion chromatograms (EIC; m/z 563.2 ± 0.3). (b) Electrospray ionization-tandem mass spectrometry (ESI-MS/MS; precursor ion, m/z 563.2, PPIX [blue diamond]) analyses showing almost identical structures of the PPIX standard and the bacterial sample.
FIG 3
FIG 3
Effects of hemH1 disruption and deletion on c-type cytochrome synthesis and nitrate reduction in PV-4. (a) Heme staining analyses of c-type cytochromes in the wild-type strain and hemH1 and hemH2 single mutants of S. loihica PV-4. After cell disruption, the supernatants containing the cellular protein fraction were resuspended in the SDS loading buffer without β-mercaptoethanol and then incubated at 37°C for 1 h. Molecular mass markers (in kilodaltons) are shown on the right. (b) Nitrate reduction of wild-type S. loihica PV-4 strain and the hemH1 deletion mutant. The parental strain carrying empty vector (PV-4/pHERD30T), the hemH1 deletion mutant carrying empty vector (PV4 ΔhemH1/pHERD30T), and the complementation strain carrying plasmid-borne hemH1 (PV4 ΔhemH1/pHERD30T-hemH1) were cultivated in the modified M1 minimal medium supplemented with 2 mM sodium nitrate under microoxic conditions (in tightly capped tubes without shaking). The blank represents the used culture medium without bacterial inoculation. The error bars represent the standard deviation (SD).
FIG 4
FIG 4
Analysis of the RpoE2-recognizing regulated promoter in Shewanella strains. (a) Sequence logos of the predicted RpoE2-dependent promoter motifs and RpoE2-dependent hemH2 gene in the S. oneidensis MR-1 and S. loihica PV-4 strains. Asterisks highlight TGATC and CGTA. (b) The induced expression of plasmid-borne rpoE2 suppressed the PPIX-overproducing phenotype of the PV4 ΔhemH1 strain and enhanced the transcription of the chromosomal hemH2 gene in the S. loihica PV-4 strain. l-Arabinose (0.01% [wt/vol]) was added to induce the expression of rpoE2, and the bacterial culture without l-arabinose was used as a control. The experiments were performed at least three times. The error bars represent the standard deviations (SD) of the results from triplicate independent samples.
FIG 5
FIG 5
Transcriptional analyses of rpoE2 and hemH paralogues in the wild-type strain and the hemH1-null mutants of S. loihica PV-4. (a) Semiquantitative RT-PCR analyses of rpoE2 and hemH2 transcripts in S. loihica PV-4 and PV-4 ΔhemH1 strains. (b) Real-time PCR analyses of hemH2 transcripts in S. loihica PV-4 and PV-4 ΔhemH1 strains. Transcription of the 16S rRNA genes was analyzed and used as the loading control. The assays were performed in triplicate, and the error bars represent the standard deviations (SD) of the results from triplicate independent samples.
FIG 6
FIG 6
Effects of hydrogen peroxide (H2O2) and visible light on the PV-4 ΔhemH1 mutant. (a) Suppression of protoporphyrin IX (PPIX) overproduction by addition of hydrogen peroxide (H2O2) and visible light irradiance in the Shewanella loihica PV-4 ΔhemH1 mutant. PPIX production in the LB broth and measurement of relative PPIX yield in terms of optical density at 405 nm (OD405). (b) Effects of hydrogen peroxide (H2O2) and visible light on the transcription of the hemH2 gene in the Shewanella loihica PV-4 wild-type strain and the PV-4 ΔhemH1 mutant. (c) Effects of hydrogen peroxide (H2O2) and visible light on the transcription of the rpoE2 gene in the PV-4 ΔhemH1 mutant. The error bars represent the standard deviations (SD).
FIG 7
FIG 7
Schematic diagram illustrating the biosynthesis pathway of heme and cellular function and transcriptional regulation of two ferrochelatase paralogues in S. loihica PV-4 strain. LPS, lipopolysaccharide; Sec, secretion; Ccm, cytochrome c maturation.

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