Helena Olivieri Individual Journal Assignment Week 3

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(Physiological Parameters:)
(Enzyme Activities:)
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===Enzyme Activities:===
===Enzyme Activities:===
*Do changes in ammonia concentrations affect enzyme activity involved in the conversion of ammonia to glutamate or glutamine? (Figure 3)
*Do changes in ammonia concentrations affect enzyme activity involved in the conversion of ammonia to glutamate or glutamine? (Figure 3)
-
*NADPH-glutamate dehydrogenase, NAD-GDH, and GS activity studied
+
*NADPH-glutamate dehydrogenase, NAD-GDH, and GS activity studied
-
*Between 29-118 mM NADPH-GDH decreased, less GDH1 expressed  
+
*Between 29-118 mM NADPH-GDH decreased, less GDH1 expressed  
-
*NADPH-GDH increased between 20 and 61 mM
+
*NADPH-GDH increased between 20 and 61 mM
-
*After 61 mM, no changes
+
*After 61 mM, no changes
*Ultimately, article suggestes that S. cerevisiae likely may have a mechanism to detect nitrogen
*Ultimately, article suggestes that S. cerevisiae likely may have a mechanism to detect nitrogen

Revision as of 00:17, 31 January 2013

Contents

The Concentration of Ammonia Regulates Nitrogen Metabolism in Saccharomyces cerevisiase

Abstract:

  • S. cerevisiase cultured with various concentrations of ammonia, effects observed
  • Relationship between extracellular ammonia and intracellular glutamate and glutamine concentrations, levels of NAD-dependent glutamate dehydrogenase activity and mRNA studied

Introduction:

  • Ammonia is nitrogenous source that encourages most rapid growth in Saccharomyces cervisiae
  • Nitrogen metabolism regulated at genetic and enzymatic levels
  • Concentration of ammonia relevant to growth activity
  • The study emphasizes the significance of having constant flux levels between cultures in order to study the effects of differing ammonia concentration.

Physiological Parameters:

  • While glucose concentration remained constant at 100 mM, S. cerevisiae concentration was studied at concentrations of 29, 44, 61, 66, 78, 90, 96, 114, and 118 mM
  • Figure 1A displays a direct correlation between ammonia concentration and biomass between 29 and 61 mM. Limited by glucose levels, concentrations higher than 61 mM did not alter biomass.
  • The overall ammonia flux into biomass was approximately 1.1 mmol/gh
  • Figure 1B displays that at ammonia concentrations above 44 mM, CO2 production and O2 consumptions remain constant.
  • Below concentrations of 44 mM, O2 consumption greatly decreased, while CO2 production increased. Residual glucose levels did not change.
  • After 29 mM, increase in ammonia concentration, therefore, did not cause relevant change to carbon metabolism.
  • Figure 1C displays the relationship between ketoglutarate, glutamate, and glutamine
  • Given incorporation of ammonia, glutamate is converted to glutamine
  • Ketoglutarate concentration is cut in half when excess of ammonia is present
  • Intracellular glutamate concentration tripled given excess ammonia
  • Glutamine concentration increases linearly

Northern Analyses:

  • Northern Blot technique used to analyze if changes were made to RNA levels of nitrogen-regulated genes
  • Figure 2 displays gene expression in relation to ammonia concentration
  • Amino acid permease-encoding genes: GAP1 and PUT4
  • Biosynthetic genes: ILV5 and HIS4
  • GDH1, GLN1, HIS4, ACT1, and H2A-H2B genes also detected through Northern Blot
  • Most GLN1, a gene that utilized ammonia, was maximized at 61 mM.
  • Ammonia concentration repressed, through gene GDH1, and induced, through GDH2, RNA expression of nitrogen-regulated genes.
  • Proline permease Put4p and Gap1p genes regulated in response to ammonia concentration
  • GAP1 and PUT4 gene RNA decreased with increase of ammonia concentration past 44 mM
  • Biosynthetic genes ILV5 and HIS4 RNA quantities increased with higher ammonia concentrations at a max of 66 mM, after 66 mM, amounts decrease

Enzyme Activities:

  • Do changes in ammonia concentrations affect enzyme activity involved in the conversion of ammonia to glutamate or glutamine? (Figure 3)
  • NADPH-glutamate dehydrogenase, NAD-GDH, and GS activity studied
  • Between 29-118 mM NADPH-GDH decreased, less GDH1 expressed
  • NADPH-GDH increased between 20 and 61 mM
  • After 61 mM, no changes
  • Ultimately, article suggestes that S. cerevisiae likely may have a mechanism to detect nitrogen
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