James P. McDonald Week 3
- Permease: "General term for a membrane protein that increases the permeability of the plasma membrane to a particular molecule, by a process not requiring metabolic energy." []
- Isomerase: "An enzyme that converts molecules into their positional isomers." []
- Oligonucleotides: "Polymers made up of a few (2-20) nucleotides. In molecular genetics, they refer to a short sequence synthesised to match a region where a mutation is known to occur, and then used as a probe (oligonucleotide probes)." []
- Dehydrogenase: "Enzyme that oxidizes a substrate by transferring hydrogen to an acceptor that is either NAD/NADP or a flavin enzyme. An enzyme that is used to remove hydrogen from its substrate, which is used in the cytochrome (hydrogen carrier) system in respiration to produce a net gain of ATP." []
- Synthetase: "Enzymes of class 6 in the e classification, catalyse synthesis of molecules, their activity being coupled to the breakdown of a nucleotide triphosphate." []
- Biosynthetic: "Relating to or produced by biosynthesis." []
- Glutamate: "Major fast excitatory neurotransmitter in the mammalian central nervous system." []
- Glutamine: "A crystalline amino acid occurring in proteins; important in protein metabolism. One of the 20 amino acids that are commonly found in proteins." []
- GAP1: "General amino acid permease, a gene found in Saccharomyces cerevisiae." []
- PUT4: "Proline permease, a gene found in Saccharomyces cerevisiae." []
- Saccharomyces cerevisiae was grown in various ammonia concentrations and the effects on the growth was observed.
- A single dilution rate was using with a range of different ammonia concentrations.
- The ammonia concentrations were varied to observe its effects on gene expression and enzyme activities.
- The main result of the study was that nitrogen metabolism is dependent on ammonia concentration, not its flux.
- Ammonia is the prefferred growth source of Saccharomyces cerevisiae as it results in faster growth.
- Nitrogen metabolism is regulated by gene expression and enzyme activity.
- Previous research seems to show that ammonia concentration itself is the most important factor in nitrogen metabolism.
- But, in these previous studies the cultures have differed in ammonium flux, leaving flux as the possible key factor.
- This experiment uses cultures with the same level flux, only the ammonium concentrations fed in are different.
- Saccharomyces cerevisiae SU32 was grown in continuous cultures
- They were fed with different ammonia concentrations: 29, 44, 61, 66, 78, 90, 96, 114, 118 mM.
- Contained a fixed glucose concentration at 100 mM.
- Had a dilution rate of 0.15h-1.
- Biomass and residual ammonia concentration were measured at the different ammonia concentrations.
- The ammonium flux was calculated using the biomass, ammonia concentration, and the residual ammonia concentration.
- The respiratory quotient was calculated using the measured values of CO2 production and O2 consumption at the different ammonia concentrations.
- Alpha-ketoglutarate, glutamate, and glutamine concentrations were measured at the different ammonia concentrations.
- RNA levels of nitrogen-regulated genes were observed to see if they changed in different ammonia concentrations.
- Used amino acid permease-encoding genes: GAP1, PUT4 and biosynthetic genes: ILV5, HIS4.
- P-labelled oligonucleotides were used to detect GDH1, GLN1, GAP1, ILV5, HIS4, ACT1, and H2A-H2B RNA levels and a separate oligonucleotide was used to analyze PUT4 RNA levels.
- A P-labelled DNA fragment was used to detect GDH2 levels and H2A-H2B was used to detect GLN1 RNA levels.
- Gene expression levels were detected using x-ray films and plotted to compare expression levels at different ammonia concentrations.
- Investigated changes in enzyme activity in different ammonia concentrations.
- Looked at enzymes involved in the conversion of ammonia into glutamate or glutamine: NADPH-GDH, NAD-GDH, and GS.
- Figure 1
- The concentrations were measured using methods from a previous paper
- In each graph the X-axis is ammonia concentration.
- Figure 1.A the y-axes are residual ammonia concentration, biomass, and ammonia flux.
- The results were determined using methods from previous papers.
- Biomass increased from 29 to 61 mM, indicating that ammonia was limiting and it leveled out above 61 mM indicating that the glucose was limiting.
- Residual ammonia only appeared after 61 mM and continually increased, showing that above 61 mM there was excess ammonia.
- The flux was kept constant to analyze the effects of changing ammonia concentrations.
- Figure 1.B the y-axes are O2 consumption, CO2 production, and respiratory quotient.
- Above 44 mM the respiratory quotient remained constant as O2 consumption and CO2 production did not vary much.
- The values only changed below 44 mM when the there was ammonia limitation.
- Figure 1.C the y-axes are concentrations of alpha-ketoglutarate, glutamate, and glutamine in the three graphs respectively.
- In the first graph the alpha-ketoglutarate decreased as ammonia concentration increased because the two reacted to produce glutamate and glutamine.
- In the next two graphs both glutamate and glutamine increased as ammonia concentration increased because both were produced by the ammonia and alpha-ketoglutarate reaction.
- Figure 2
- Gene expression levels were detected using an x-ray film method described in a previous paper.
- In each graph the X-axis is the ammonia concentration.
- In each graph the Y-axis is percentage of RNA expression of each gene.
- GDH1 expression stayed constant until 78 mM when it decreased.
- GDH2 expression was not detected until 44 mM where it then increased greatly after 61 mM.
- GAP1 and PUT4 expression were similar, they were both constant until 44 mM where they decreased greatly after that.
- GAP1 and PUT4 are both impacted by ammonia concentration and not flux.
- GLN1, HIS4, and ILV5 all follow a similar trend, increasing until about 80 mM and then decreasing there after.
- James P. McDonald
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