Part:BBa_K5378000

glutamine synthetase

The glutamine synthetase (GS) is an ammonia scavenger that is located in perivenous hepatocytes (constituting around 6–7% of the parenchymal population) and catalyses the ATP-dependent amidation of glutamate to glutamine. There are documents proving that hepatic deletion of GS in mice results in hyperammonaemia, oxidative stress in brain tissue, behaviour abnormalities and reduced lifespan.

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  COMPATIBLE WITH RFC[21]
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  COMPATIBLE WITH RFC[1000]

Usage and Biology

In humans and other mammals, ammonia is majorly digested by the Urea Cycle in the liver. However, as it is shown before, the liver functions are destroyed in HE patients, so the urea cycle is hard to use. So we move our sight to plants. Plants utilize ammonium (NH₄⁺) as a nitrogen source through several processes, which are critical for their growth and development. Upon uptake by plant roots, ammonium is either directly assimilated into amino acids via the glutamine synthetase-glutamate synthase (GS-GOGAT) pathway or converted to nitrate for further use in metabolic processes. Ammonium is an energetically favorable form of nitrogen compared to nitrate(like the annamox bateria), as it does not require reduction before assimilation. However, excessive ammonium can be toxic to plants, so its uptake and assimilation are tightly regulated to maintain optimal nitrogen levels within the plant tissues. As for the nitrate path, it may produce harmful side products such as nitrite, so we finally decided to mimic the GS-GOGAT cycle to metabolize ammonia in HE patients. So we expressed the glutamate synthase in EcN, and it can degrade ammonia into glutamine without harm to the body.

Figure 1. CAPTION_HERE

Functional Verification

Ammonia degrading ability of GS enzyme

Our metabolic module aims to degrade the over-accumulated NH3 in patients' gut by expressing GS, an enzyme that could utilize NH4+ and metabolize it into glutamine which does no harm to the human body. To validate the feasibility of this module, we transformed EcN with plasmid Ptac-GS and used IPTG to induce the expression of GS (Figure 2a). Meanwhile, we transformed EcN with the vector plasmid PET-32a as control gruop and coculture them with differnt concentratioon of NH4Cl in M9 minimal culture medium.

To our joy, the ammonia level in EcN_GS group cocultured with 50μM NH4Cl for 12 hours is significantly lower than the control group (Figure 2b), and this trend remains when we extended coculturing time to 24 hours (Figure 2c). These results indicate the successful expression and function of the metabolic module.

Altogether: Sensing-Metabolic System Validation

To demonstrate the function of our system after assembly, we co-transformed EcNs with plasmid Pcon-tynA-Pcon-feaR and plasmid PTynA-GS and coculture the engineered bacteria with different concentrations of PEA and NH4Cl (Figure 3a). Results showed that with the concentration of 50μM NH4Cl, 100ng/ml PEA induced the most significant decrease in ammonia (Figure 3b), which was consistent with the trend in both sensing and metabolic modules.

We also transformed plasmid Pcon-tynA-Pcon-feaR into EcN as the control group, and cocultured them with 100ng/ml PEA and 50μM NH4Cl for 4,8,12 and 24 hours. Results demonstrated a significant ammonia decrease in experiment group compared with the control group (Figure 3c), indicateing that a rahter high level of PEA could iniitate downstream metabolic module to express GS and resulted in the decrease of over-accumulated ammonia.

Figure 2. CAPTION_HERE

Reference

[1]Qvartskhava, N. et al. Hyperammonemia in gene-targeted mice lacking functional hepatic glutamine synthetase. Proc. Natl Acad. Sci. USA 112, 5521–5526 (2015).

[2]Frieg, B., Gorg, B., Gohlke, H. & Haussinger, D. Glutamine synthetase as a central element in hepatic glutamine and ammonia metabolism: novel aspects. Biol. Chem. 402, 1063–1072 (2021).

[3]Paluschinski, M. et al. Characterization of the scavenger cell proteome in mouse and rat liver. Biol. Chem. 402, 1073–1085 (2021).

[4] Haussinger, D. Nitrogen metabolism in liver: structural and functional organization and physiological relevance. Biochem. J. 267, 281–290 (1990).

[5]Gallego-Durán, R., Hadjihambi, A., Ampuero, J. et al. Ammonia-induced stress response in liver disease progression and hepatic encephalopathy. Nat Rev Gastroenterol Hepatol (2024). https://doi.org/10.1038/s41575-024-00970-9

[6]Hao DL, Zhou JY, Yang SY, Qi W, Yang KJ, Su YH. Function and Regulation of Ammonium Transporters in Plants. Int J Mol Sci. 2020 May 18;21(10):3557. doi: 10.3390/ijms21103557. PMID: 32443561; PMCID: PMC7279009.