Testing the Potential of Regulatory Sigma Factor Mutants for Wastewater Purification or Bioreactor Run in High Light
| Autor: | Esa Tyystjärvi, Taina Tyystjärvi, Juha Kurkela, Dimitar Valev |
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| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: |
Transcriptional Activation
Light Sigma Factor Biology Applied Microbiology and Biotechnology Microbiology Article Water Purification 03 medical and health sciences chemistry.chemical_compound Bioreactors Bacterial Proteins Sigma factor Bioreactor Ammonium 030304 developmental biology HEPES 0303 health sciences Growth medium Strain (chemistry) 030306 microbiology Synechocystis General Medicine Gene Expression Regulation Bacterial Phosphate 6. Clean water Culture Media Oxidative Stress chemistry Biochemistry Wastewater Mutation |
| Zdroj: | Current Microbiology |
| ISSN: | 1432-0991 0343-8651 |
| Popis: | It is shown that a freshly inoculated culture of the model cyanobacterium Synechocystis sp. PCC 6803 consumed almost all phosphate and 50% of nitrate within 6 days from the nutrient-rich BG-11 growth medium, indicating potential of cyanobacteria to purify wastewaters. Synechocystis sp. PCC 6803 control strain also collected nutrients efficiently from a landfill leachate wastewater KA2 (5.9–6.9 mM ammonium and 0.073–0.077 mM phosphate). Wastewaters might induce oxidative stress to microalgae, which prompted us to test growth of sigma factor inactivation strains, as ΔsigBCE and ΔsigCDE strains show superior growth in chemically induced oxidative stress. All cyanobacterial strains, including a stress-sensitive strain ΔsigBCDE, grew well in KA2 for four days, indicating that KA2 did not cause immediate oxidative stress. Completely arrested growth and bleaching of ΔsigBCDE cells after one week in KA2 wastewater point to the importance of group 2 sigma factor-mediated changes in gene expression during wastewater treatment. The growth of ΔsigBCD was arrested early in un-buffered and Hepes buffered (pH 7.5) KA2. In ΔsigBCD, all phosphate transporter genes are upregulated in standard conditions, and ΔsigBCD cells showed growth defects in low-phosphate BG-11 medium. ΔsigBCD cells removed phosphate slower from KA2 than the control strain, but phosphate supplementation of KA2 did not improve growth of ΔsigBCD. The ΔsigBCE strain showed superior growth in a laboratory-scale bioreactor in bright light and removed phosphate even slightly more efficiently than the control strain if KA2 was Hepes buffered although ΔsigBCE grew slowly in un-buffered KA2 and in low-phosphate BG-11 medium. The results indicate that engineering expression of regulatory group 2 sigma factor(s) might be useful for practical applications. Electronic supplementary material The online version of this article (10.1007/s00284-020-01973-w) contains supplementary material, which is available to authorized users. |
| Databáze: | OpenAIRE |
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