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Energy Metabolism - Georgia Institute of Technology
Energy Metabolism - Georgia Institute of Technology

Chapter 2b
Chapter 2b

... • Lower the activation energy, increase the speed of a reaction (millions of reactions per ...
Metabolism of lipids
Metabolism of lipids

... • The FAs are built by sequential addition of two-carbon units derived from acetyl CoA. The activated donor of the two-carbon units in the elongation step is malonyl-ACP (a three-carbon unit) but during the elongation, CO2 is released. This drives the reaction • The reducing agent is NADPH. • Elonga ...
Lecture 3 - Glycolysis and Gluconeogenesis 1 2 3 4
Lecture 3 - Glycolysis and Gluconeogenesis 1 2 3 4

Lecture 3 - Glycolysis and Gluconeogenesis
Lecture 3 - Glycolysis and Gluconeogenesis

Amino Acid Synthesis
Amino Acid Synthesis

... b. There are 10 essential amino acids we cannot make. c. Looking back in evolution, why is it that bugs can make all these and we can’t? It turns out that one thing you can look at is how badly we need them and how difficult it is to make them. d. We do not need any of them because we cannot get the ...
Lab Module 7 - philipdarrenjones.com
Lab Module 7 - philipdarrenjones.com

... In Lab Module 1, we applied the scientific method to test factors that affect reaction time. This week, we will again use the scientific method, this time to test factors that affect the rate of fermentation by baker’s yeast, Saccharomyces cerevisiae as well as fermentation in humans. Fermentation i ...
The urea cycle
The urea cycle

... production (the total lack of any cycle enzyme results in death shortly after birth). Rather, the deficient enzyme's substrate builds up, increasing the rate of the deficient reaction to normal. The anomalous substrate buildup is not without cost, however. The substrate concentrations become elevate ...
The acetaminophen metabolite
The acetaminophen metabolite

... was added to 5-50 μL of NAPQI (1 g/L in 5% acetonitrile/ammonium bicarbonate) and incubated at 37ºC for 1 h. The reaction mixture was lyophylised using a centrifugal evaporator, and resuspended in 15 μL of NuPAGE LDS sample buffer without dithiothreitol (Novex; Life Technologies, Paisley, UK). The e ...
1 PERKINELMER™ LIFE SCIENCES, INC. OLIGONUCLEOTIDE 5
1 PERKINELMER™ LIFE SCIENCES, INC. OLIGONUCLEOTIDE 5

... steps that are involved in the cloning and isolation of restriction fragments to be used as hybridization probes. Another advantage of oligonucleotide probes is that they can be designed to detect single base changes (mutations) in a gene1-5. This is an especially useful property, by adjusting the c ...
Citrate synthase proteins in extremophilic organisms: Studies within
Citrate synthase proteins in extremophilic organisms: Studies within

... native structures and sequences of amino acids. An evolutionary divergence from a common ancestor may lead diverse sequences to fold to nearly the same native structure. One particularly interesting example is citrate synthase (CS), an enzyme that is found in most living organisms, from bacteria to ...
Citric Acid Cycle
Citric Acid Cycle

... final common pathway for oxidation of fuel molecules  provides intermediates for biosynthesis ...
File
File

... • Energy must be expended to put an additional negatively charged phosphate on ADP ...
short chain polypeptide test
short chain polypeptide test

... permeability (leaky gut syndrome) or inadequate digestion (enzymes and acid). Amino acids are the basic building blocks of very large molecules called proteins. When two or more amino acids are joined together they are called peptides. So called ‘short-chain polypeptides’ are up to around 30 amino a ...
The role of xylulokinase in Saccharomyces cerevisiae xylulose
The role of xylulokinase in Saccharomyces cerevisiae xylulose

... the forward reactions were about 600 nkat mg31 (640 with D-xylulose, 500 with ATP). Km and Vmax were obtained from Hanes^Woolf plots of the presented data. All these data were obtained under similar conditions at the same pH (pH 6.5). From these data, an equilibrium constant of 90 was calculated usi ...
III. Metabolism
III. Metabolism

... Two enzymes involved: Pyruvate decarboxylase irreversible Alcohol dehydrogenase reversible Regenerates NAD+ from NADH (reducing equivalents) produced in glycolysis. Pathway is active in yeast Second step is reversible → ethanol oxidation eventiually yields acetate → enters fat synthesis ...
Bioenergetics Objectives Objectives
Bioenergetics Objectives Objectives

... • Describe how metabolic pathways are regulated • Discuss the interaction of anaerobic & aerobic ATP production during exercise • Identify the rate limiting enzymes ...
Distribution and phylogenies of enzymes of the Embden
Distribution and phylogenies of enzymes of the Embden

... domains, although there is significant variation in enzymes, especially in the Archaea and in hyperthermophilic bacteria (Fothergill-Gilmore and Michels 1993, Schönheit and Schäfer 1995, Selig et al. 1997, Ronimus and Morgan 2001). Several reviews of the distribution of glycolytic enzymes were publi ...
03-232 Biochemistry         ... Name:________________________ or the back of the preceding page.  In questions... Instructions:
03-232 Biochemistry ... Name:________________________ or the back of the preceding page. In questions... Instructions:

... 13. (12 pts) Please do one of the following three choices. If appropriate you should state the type of regulation (feedback, product, allosteric) in your answer. Choice A: Glycolysis, gluconeogenesis, and the TCA cycle are all regulated by “energy sensing”. Select one of the three pathways and descr ...
M-path: a compass for navigating potential metabolic pathways
M-path: a compass for navigating potential metabolic pathways

... using group contribution method (Jankowski et al., 2008). The thermodynamics data used in this work are shown in Supplementary Table S2, and we used this option in this work. ...
Proteins and their Ligands: Their Importance and how to Crystallize
Proteins and their Ligands: Their Importance and how to Crystallize

ACTIVE SITES OF HEMOPROTEINS
ACTIVE SITES OF HEMOPROTEINS

... C. Active site of lignin peroxidase Lignin peroxidase (LiP) and manganese-dependent peroxidase (MnP), both isolated from Phanerochaete chrysosporiwn, are the two heme peroxidases which are involved in lignin biodegradation (Tien and Kirk, 1983; Glenn et al, 1983; Glenn and Gold, 1985). LiP exists as ...
Ch 9 Kreb Cycle and ETC
Ch 9 Kreb Cycle and ETC

... u  if O2 is available, pyruvate enters mitochondria u  enzymes of Krebs cycle complete the full oxidation of sugar to CO2 u  ...
File
File

... •The pyridine ring is stable to metabolism •The pyridine ring is a good leaving group (neutralisation of charge) •Exists as a zwitterion and is soluble in water •Poorly absorbed through the gut wall •Administered by injection ...
PpASCL, a moss ortholog of antherspecific chalcone synthaselike
PpASCL, a moss ortholog of antherspecific chalcone synthaselike

... (PKSs), also known as anther-specific chalcone synthase-like enzymes (ASCLs). Chalcone synthase (CHS) and other type III PKSs produce a variety of secondary metabolites in plants and microorganisms by catalyzing the condensation reactions of a starter-CoA and malonyl-CoA substrates and the cyclizati ...
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Enzyme



Enzymes /ˈɛnzaɪmz/ are macromolecular biological catalysts. Enzymes accelerate, or catalyze, chemical reactions. The molecules at the beginning of the process are called substrates and the enzyme converts these into different molecules, called products. Almost all metabolic processes in the cell need enzymes in order to occur at rates fast enough to sustain life. The set of enzymes made in a cell determines which metabolic pathways occur in that cell. The study of enzymes is called enzymology.Enzymes are known to catalyze more than 5,000 biochemical reaction types. Most enzymes are proteins, although a few are catalytic RNA molecules. Enzymes' specificity comes from their unique three-dimensional structures.Like all catalysts, enzymes increase the rate of a reaction by lowering its activation energy. Some enzymes can make their conversion of substrate to product occur many millions of times faster. An extreme example is orotidine 5'-phosphate decarboxylase, which allows a reaction that would otherwise take millions of years to occur in milliseconds. Chemically, enzymes are like any catalyst and are not consumed in chemical reactions, nor do they alter the equilibrium of a reaction. Enzymes differ from most other catalysts by being much more specific. Enzyme activity can be affected by other molecules: inhibitors are molecules that decrease enzyme activity, and activators are molecules that increase activity. Many drugs and poisons are enzyme inhibitors. An enzyme's activity decreases markedly outside its optimal temperature and pH.Some enzymes are used commercially, for example, in the synthesis of antibiotics. Some household products use enzymes to speed up chemical reactions: enzymes in biological washing powders break down protein, starch or fat stains on clothes, and enzymes in meat tenderizer break down proteins into smaller molecules, making the meat easier to chew.
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