Biochemistry Extracellular Enzymes Lab All organisms convert small organic compounds, such as glucose, into monomers required for the production of macromolecules; e.g., Building Blocs Monomers Macromolecules Glucose Glucose-6-P Pentose-5-P Pyruvate Acetyl-CoA xalacetate Erythrose-4-P etc Fatty Acids Sugars Amino Acids Nucleotides Lipids Glycogen Proteins RNA DNA
Metabolism The synthesis of building bloc compounds, monomers and macromolecules from glucose (and other simple compounds, such as C ) is conducted by the metabolic reactions of the cell, such as the highly abbreviated synthesis of amino acids shown here: EMP Pathway Pentose Phosphate Pathway Glucose (C 6 ) Pentose (C 5 ) istidine (C 6 ) Glycine (C ) Serine (C 3 ) Cysteine (C 3 ) Triose (C 3 ) Tetrose (C 4 ) Alanine (C 3 ) Lysine (C 6 ) Pyruvate (C 3 ) AcetylCoA (C ) Shiimate (C 7 ) Phenylalanine (C 9 ) Tyrosine (C 9 ) Tryptophan (C 11 ) Methionine (C 5 ) Aspartate (C 4 ) Threonine (C 4 ) Isoleucine (C 6 ) aa (C 4 ) Citrate (C 6 ) TCA Cycle xoglutarate (C 5 ) Valine (C 5 ) Leucine (C 6 ) Phenylalanine (C 9 ) Tyrosine (C 9 ) Tryptophan (C 11 ) All of these reactions, of which there are more than 1000, are catalyzed by enzymes.
Amino Acids
More Complete Metabolic Networ TP
Chemical Potential Enzymes Enzymes are large proteins that all organisms synthesize to catalyze metabolic reactions. Enzymes are typically highly specific, converting only one substrate to one product. Almost all reactions that occur within the cell, including energy production (catabolism) and biosynthesis (anabolism), are catalyzed by enzymes. Reactions that are thermodynamically unfavorable (i.e., endoergic) require an energy source, such as ATP to proceed. Catalysts AB Reaction: A B A Energy released by reaction E A without catalyst B E A with catalyst Activation energy, E A, must be supplied to most reactions in order for them to proceed. A catalyst lowers the activation energy, allowing a reaction to proceed at lower temperatures. Catalysts are neither consumed nor produced in the reaction. Enzymes are a class of catalysts Reaction Extent Broc: pp. 110-11, Sec. 4.5
Enzyme Catalysis The sequence of amino acids that comprise enzymes convey a 3D structure that: Allows only specific substrates and cofactors to bind with the enzyme Aligns the substrate with the reaction center of the enzyme The 3D enzyme structure and catalytic activity can be lost by exposing the enzyme to high temperatures, salinity, p, and other extremes. These extremes denature the enzyme. Many enzymes have a reaction center that contains a metal cofactor, such as Mg, Mo, Cu, Fe, etc. Regulatory (or allosteric) enzymes are affected by other compounds (modulators) that can either inhibit or activate an enzyme s catalytic properties. Enzyme Substrate Modulator Mo Mo Reaction Center With modulator, enzyme can bind with substrate to produce product Without modulator, enzyme can not bind with substrate
Bovine ribonuclease A hydrolyzes RNA during digestion space-filling model of RNAse A with a bound substrate ribbon model of the protein bacbone substrate binding site For molecular structures and imaging see http://pdbwii.org/ http://www.umass.edu/microbio/chime/top5.htm http://rasmol.org/ http://polyview.cchmc.org/polyview3d.html http://www.ncbi.nlm.nih.gov/structure particulate methane monooxygenase
Reaction Kinetics Elementary Reactions Reaction rder Rxn Rate Units of A B First V = [A] d -1 A + B C Second V = [A][B] d -1 M -1 Complex Reactions bserved: A F Propose mechanism consisting of elementary reactions: A B + C B D C E D + E F Derive reaction inetics d[ F] V 4[ D][ E] dt Need to solve for [D] and [E], etc so that given the concentration of A, the overall reaction rate can be determined.
Enzyme Kinetics Mechanism 1 E + S ES Enzyme binds w/ substrate -1 S E P ES E + P Enzyme releases product Kinetic equations V o = [ES] Reaction rate. d [ ES] 1[E][S] 1[ES] dt [ES] [E T ] = [E] + [ES]; where [E T ] is the total amount of enzyme present. Analytical solution is not possible with above equations; however, Steady state assumption turns out to be good approximation d[es] dt 0
Derivation [ES] [E][S] [ES] [ES] [E][S] ES 1 1 1 1 SSA dt d ] [ ] [ ] [ ] [ ES E E T [ES] [S] ]-[ES] [E 1 T 1 [S] ][S] [E [S] ][S] [E [ES] 1 1 T 1 1 T 1 [S] ][S] [E [ES] v 1 1 T o
Michaelis-Menten Kinetics The four inetic equations can be solved to give: V o V K M [S] [S] MAX where V K MAX M 1 1 [E T ] Maximum reaction rate Michaelis-Menten constant, or half saturation constant V MAX Reaction rate, V o When [S] = K M, V o = ½V MAX Asymptotes As [S] ; V o V MAX MAX V As [S] 0; V o [S] [S] K M K M [S]
a, b Michaelis-Menten versus 1 st order inetics r r a, b First rder Kinetics Michaelis-Menten Kinetics 10 8 6 4 0 r = 1 [A]; 1 = 1 0 4 6 8 10 A MAX V [A] r ; V K [A] MAX = 1, K M = 1 0.8 0.6 0.4 0. 0 M 0 4 6 8 10 A 10 8 6 4 0 d[a] r; dt B A d[b] r dt 0 5 10 15 0 Time A B 10 8 6 4 0 d[a] r; dt d[b] r dt B A 0 5 10 15 0 Time Note, for Michaelis-Menten inetics the increase in [B] and the decrease in [A] occurs linearly while [A] >> K M Can use linear increase to measure V MAX
Transport across the cell membrane The concentration of substrates outside the cell are usually at low concentration, i.e. nm The concentration of substrates inside the cell are usual at high concentrations, i.e. mm Consequently, the cell must actively transport material across the cell membrane. Special proteins embedded in the cell wall and membrane are responsible for transporting material into and out of the cell. These transport systems only operate on relative small molecules, i.e. < 1000 MW Transport proteins utside Cell Inside Cell See Broc, pp. 63-67 Sec. 3.6
Peptidoglycan Example (E. coli) NAG N-acetylglucosamine NAM N-acetylmuramic acid NAG is also the monomer of chitin
Possible Lignin Structure
Diagenetic Reactions
Bacterial Substrates All organisms are comprise of mostly polymeric material: protein, cellulose, starch, lipids, peptidoglycans, lignin, RNA, DNA, etc. Consequently, dead organic material available for bacterial consumption is mostly large polymeric material with high molecular weights. Large polymeric compounds can not be transported across the cell wall. As organic material is exposed to environmental factors, such as ultraviolet light, absorption onto minerals (clay, etc) and bacterial degradation, the organic material becomes even more amorphous. Problem: monomers exist at low concentration and mae up only a small percent of the extracellular PM+DM pool. ow do bacteria breadown and consume the large polymeric material?
Extracellular Enzymes In order to breadown large polymeric organic material into small monomers, bacteria produce extracellular and ectoenzymes. Extracellular Enzymes: Excreted from cell and exist in solution in free form. Ectoenzymes: Bound to cell surface, but can attac extracellular substrates. Both types of enzymes are produced by both Gram negative and Gram positive bacteria Gram Negative Gram Positive membrane cell wall membrane periplasmic space See Broc, pp. 69-75 Sec. 3.7-3.8 Bacterial growth may often be limited by the hydrolysis rate of extracellular macromolecules (area of current research).
Gram Negative Cell Wall Diagram
Enzyme Assay Extracellular and ectoenzymes catalyze hydrolysis reactions, which are exoergic, so do not require an energy source, such as ATP, to proceed: -A-A-A-A- + -A-A- + -A-A- Because of the low concentrations of the substrates, it is not practical to measure the decrease in concentration of the natural substrates. Fluorogenic substrates are used as analogs to the true substrates. MUF-R: 4-methylumbelliferyl-R MUF: 4-methylumbelliferyl R Any molecule + R- + - Fluoresces C 3 C 3 MUF fluoresces provided nothing is bound to -. At low p, MUF will become MUF- and will not fluoresce. By using different molecules bound to MUF (i.e., -R), different enzymes can be assayed.
MUF Enzyme Assays Endopeptidase N C C R N C C R + N C C R + N C R C Assay substrate: L-Leucine-7-amido-4-methylcoumarin hydrochloride Phosphatase R--P 3 - + R- + P 4 - Assay substrate: MUF-phosphate
More MUF Enzyme Assays -1,4-glucosidase (cellobiase) C C + Glucose Assay substrate: MUF--D-glucoside N--D-acetyl-glucosaminidase (Chitobiase) C N C + N-acetyl-glucosaminide N C= C= C 3 C 3 Assay substrate: MUF-N--D-acetyl-glucosaminide
Eco- and Extracellular Enzyme Assay MUF Conc. (nm) Introduce MUF substrate for enzyme to be assayed Measure accumulation of free MUF with fluorometer over time. Plot MUF concentration versus time (mae sure to account for dilution). Determine slope of line that best fits the data. This slope is V MAX d [MUF ] V MAX dt Enzymes Assayed: Chitobiase Phosphatase Endopeptidase Cellobiase Time (h) ow might V MAX be used to determine the state of an ecosystem? Note, the enzyme activity measured is not the activity that occurs in the natural environment! Why?
Example Applications From: Chróst, R.J. (1991) Microbial enzymes in aquatic environments.