proteins 3 Flashcards

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1
Q

what is the Gibbs free energy equation

A

G= H-TS
H= enthalpy
S= entropy
T= temperature in K

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2
Q

what is Gibbs free energy

A

amount of energy available to do work

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3
Q

what time of reaction is it if Gibbs free energy is positive or negative

A

positive - endergonic
negatie - exergonic

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4
Q

what are the standard conditions

A
  • 1 molar concentrations
  • 1 atm
  • 25 degrees of 298 k
  • pH7
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5
Q

what is the equilibrium constant equation

A

Keq= product concentration / reactant concentration

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6
Q

link Keq to the Gibbs free energy equation

A

G= G(standard free energy) + RTInKeq
simplified to G= -R x Tx InKeq

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7
Q

if the standard reduction potential is more positive it means…

A
  • stronger oxidising agent - electron acceptor
  • weaker reducing agent
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8
Q

if the standard reduction potential is more negative it means…

A
  • weaker oxidising agent
  • stronger reducing agent
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9
Q

how does the standard electrode potential work

A
  • reference cell = 0 volts
  • electrons transferred through agar bridge and wire
  • electron direction depends on relative redox power
  • initial voltage taken at beginning of experiment when concentration is 1 mole
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10
Q

what does epinephrine do in the body and where is it from

A
  • from adrenal medulla and nerve endings
  • used in liver for glycogenolysis and fat breakdown
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11
Q

where is glucagon from and what does it do in the body

A
  • from pancreatic alpha cells
  • used in liver for glucogenolysis
  • used in adipose for triacylglycerol breakdown
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12
Q

where is cortisol from and what does it do in the body

A
  • from adrenal cortex
  • used in muscle and adipose for insulin resistance
  • increases liver gluconeogenesis
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13
Q

how is insulin released into the blood

A

1) glucokinase repsons to glucose in glycolysis
2) ATP produced in mitochondria
3) ATP-sensitive potassium channels close
4) change across membrane potential
5) calcium gates open
6) insulin vesicles fuse with membrane
7) insulin released into blood

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14
Q

what causes primary lactase deficiency

A
  • genetic fault of MCM6 regulator at LCT
  • less reliant on milk so decreased expression
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15
Q

what causes secondary lactase deficiency

A
  • problems with small intestine eg. infections, crohns disease
  • have lactose free products, extra calcium and vitamin D and lactase substitutes
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16
Q

what does SGLT1 transporter do

A
  • glucose and galactose
  • against concentration gradient
  • Na+ symporter
  • from intestinal lumen to epithelial
17
Q

what does GLUT5 transporter do

A
  • fructose
  • inefficient
  • intestinal lumen to epithelial
18
Q

what soda GLUT2 transporter do

A
  • glucose , galactose and fructose
  • epithelial to capillary
19
Q

what causes a GLUT 4 deficiency and what are the symptoms

A
  • mutation in SLC2A4 in muscle and fat cells
  • causes type 2 diabetes
  • high blood sugar, insulin release stimulated, reduced glucose uptake
20
Q

what causes a GLUT 2 deficiency and what are the symptoms

A
  • mutation of SLC2A2 in liver and pancreatic B cells
  • causes type 2 diabetes
  • fanconi-bickel syndrome - autosomal recessive - impaired glucose - glycogen accumulation and renal dysfunction
21
Q

what causes a GLUT1 deficiency and what are the symptoms and treatment

A
  • mutation in SLC2A1 - autosomal dominat
  • first month of life, nervous system disorder, small head, frequent seizures, developmental delay
  • treatment of ketogenic diet - high fat, moderate protein and low carbs
22
Q

what causes a SGLT1 deficiency and what are the symptoms

A
  • murrain in SLC5A1
  • in infancy
  • severe diarrhoea, weight loss, mild glucosuria, kidney stones