Part:BBa_K4816012
Nitrous Oxide Reductase (NosZ) from Paracoccus denitrificans PD1222
Biological Background
Denitrification is a vital component of the nitrogen cycle, a biological process that converts nitrates and nitrites into nitrogen gas, ultimately returning nitrogen to the atmosphere. This cycle is primarily orchestrated by various types of bacteria, and denitrification can occur under two distinct conditions: aerobic and anaerobic.
Aerobic denitrification, in particular, is facilitated by specific bacteria that contain a set of four critical enzymes located in the periplasm. These enzymes play pivotal roles in the denitrification process:
- Nitrate Reductase (NapA) BBa_K4816009
- Nitrite Reductase (NirS) BBa_K4816011
- Nitric Oxide Reductase (NorB) BBa_K4816010
- Nitrous Oxide Reductase (NosZ) BBa_K4816012
The Denitrifying cycle consists of a series of reactions that lead to the production of nitrogen gas, the biochemical pathway is a four-step process where first nitrate (NO3-) is reduced to nitrite (NO2-) by nitrogen reductase, the catalytic active part expressed by the gene napA, then nitrite is further reduced to nitric oxide (NO) by nitrite reductase (nirS), nitric oxide is reduced to nitrous oxide (N2O), which is a potent greenhouse gas, by the enzyme nitric oxide reductase (norB), finally the limiting step of the pathway is the reduction of nitrous oxide into nitrogen gas (N2) by the enzyme nitrous oxide reductase (nosZ). As shown in equation 1.
Equation 1: Denitrifying cycle shown as a serie of biochemical equilibrium reactions.
One notable bacterium frequently employed in denitrification studies is Paracoccus denitrificans. The preference for Paracoccus denitrificans over organisms like Pseudomonas aeruginosa is often due to the latter's pathogenic nature. Paracoccus denitrificans, on the other hand, is non-pathogenic and can serve as a safer model for denitrification research.
Additionally, Paracoccus denitrificans holds further significance in the context of synthetic biology. This bacterium is more closely related to cyanobacteria, photosynthetic organisms capable of harnessing solar energy to convert carbon dioxide into organic compounds. This connection suggests the potential for future applications in synthetic biology, where Paracoccus denitrificans enzyme may be engineered to enhance environmental sustainability and resource utilization using Cyanobacteria chasis.
To get more information about the project visit the wiki iGEM Bonn-Rheinbach 2023: NitraNix
Gene Isolation
Paracoccus denitrificans PD1222 gene encoding for NosZ part of the chromosome 2 (NCBI ID: CP000490.1) located between base pairs (1380640 and 1382598). NosZ is the active subunit of the nitrous oxide reductase. This modified gene contains two unique restriction sites, NdeI flanking the 5' terminus and XhoI flanking the 3' terminus. Using the primers foward BBa_K4816006 and reversed BBa_K4816007 to obtain the gene of interest by PCR from Paracoccus denitrificans PD1222 plasmid DNA. The restriction site addition allows the insertion into different vectors. In this case, we use them to insert in the plasmid pet 23 a (+) to further protein expression and isolation, because the plasmid add a His-Tag to the C-terminus of the protein. Important to notice the deletion of the stop codon.
Usage and Biology
NosZ was obtained by PCR amplification of genomic DNA at 45°c obtaining a prominent band at nearly 2kb.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NotI site found at 600
Illegal NotI site found at 1937 - 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 1969
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 85
Illegal NgoMIV site found at 117
Illegal NgoMIV site found at 160
Illegal NgoMIV site found at 922
Illegal NgoMIV site found at 1282 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 34
Illegal BsaI.rc site found at 1600
//cds/enzyme
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