Cell Fractionation
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Cell Fractionation
Summary & Revision
Experimental animals
Rats , mice , rabbits , guinea pigs
Kreb's Cycle
(Tricarboxylic acid cycle ( TCA
Citric acid Cycle
ATP = Biological battery
(NAD : nicotineamide adenine dinucleotide ( oxidized form
( reduced form )
: NADP
Energy charges
↑ ATP
AMP + 2 P = ATP
ADP + P = ATP
ADP , AMP
NADH , NAD
1 ما المقصود ؟؟
هل يمكن عزل جميع عضيات الخلية في صورة سليمة ؟؟؟
عزل النواة - التحقق من عزل النواة
عزل الميتوكوندريا - التحقق
عزل الميكروسومات و الليسوسومات - التحقق
عزل السيتوسول – التحقق
تقنية الطرد المركزي - النواع – الخصائص
النزيمات - فكرة عامة - كيفية تقديرها – نشاطية النزيم
الحسابات و النتائج
M – 0.34 M Sucrose solution 0.25
M.W = 342
ml 100
g = 0.25 * 342 * 100 / 1000
g / 100 ml 8.5
For osmotic pressure
2 MCQ : Multiple Choice Questions
Sucrose
Carbohydrate
Disaccharide
Table sugar
Glucose + Fructose
C6 H12 O6 72 + 12 + 96 = 180
Isomers
3 Crude DNA
Diphenyl amine R. ( R. = Reagent )
DNA ------Deoxyribose ------(HCl) _____ Furfural derivative
( diphenyle amine ) ______Bluish color
Standard DNA ( Calf thymus )
Crude RNA
Orcinol ------ribose ------(HCl) _____ Furfural derivative
( orcinol ) ______Blue – green color
Confirmatory Tests
Tm : melting temperature
Nitrogenous bases A , C , G , T , U
260 – 280 nm ( U.V. region ) ultra violet
U.V. absorption method for Nucleic acids ( for pure samples )
تنقية Purification
Nucleoproteins ( conjugated protein)
Histones
1% E 1Cm for DNA at 260 nm = 200 ( Calf Thymus )
1g / 100 ml
1000 mg / 100 ml
4 10 mg / 1 ml ____ 200
1mg / 1ml ______20
0.1 mg / 1 ml ______2.0
0.01 mg / 1 ml ______0.20
1% E 1Cm for RNA at 260 nm = 250 ( yeast )
Results :
? mg DNA ( or RNA) / g liver dry tissue
أنواع كروماتوجرافيا العمود Column chromatography
( .Gel filtration ( based on mol.wt
( Ion exchange chromatography ( charge
Affinity chromatography
5 Kreb's cycle
.β Oxidation of f.as
Oxidative phosphorylation
( ETC ( electron transport chain
IDH isocitrate dehyrogenase
Microsomes
( Ultracentrifuge ( 75,000 r.p.m
Beckmann
(Mixed function oxidases ( MFO
eg : aldehyde oxidase , xanthine oxidase , Cyt P450
Cytosol
( High speed centrifuge ( 15000 – 18,000 rpm
( Sorvall ( American company
6 Glycolysis
Glucose ______pyruvate
Pyruvate + NADH ______lactate + NAD
LDH : lactate dehydrogenase
RCF : Relative centrifugal force
xg = ??? rpm 45,000
E , S , P , PH , T
S : Substrate
E : Enzyme
T:Temperature
In-vitro
In-vivo
Enzyme assay
Amylase
Starch ( MW 1.5 * 10 6 ) ______Dextrins ______Disaccharides ( maltose & isomaltose ) ______Glucose ( ( reducing sugar
7 ( C6H12O6 ( 72 + 12 + 64 = 180
µ mole produced / min / ml E = U / ml U : unit
DNS 3,5
Dinitrosalicylate , yellow – orange in color ( color R for reducing 3,5 ( sugars
0504677397
The reducing sugar will reduce NO2 group in position 3 to NH2
The color will be changed from yellow orange into red
DNS has two functions
To stop the enzymatic reaction ( DNS is prepared in 2M Na OH )
Will react with glucose produced
Cytology
Eukaryotes
Organelles
Plasma membrane
Nucleus
Cytoplasm = cytosol
Mitochonderia
8 Ribosomes
Endoplasmic reticulum
Golgi apparatus
Nucleolus
Rat liver ( 1 g )
0.25 M sucrose
Homogenization ( Homogenizer ) 1:5
Centrifugation ( Centrifuge )
1. Bench- Top centrifuge ( up to 6000 rpm ) rpm : round per minute
2. High speed centrifuge ( up to 20000 rpm )
Sorvall : American company
3. Ultra centrifuge ( up to 100000 rpm )
Physiological Saline = 0.9% NaCl
9 Dehydrogenases enzymes e.g . isocitrate dehyrogenase alpha – ketoglutarate dehydrogenase
Oxidoreductases E.C.1
Enzyme Commission pyruvate dehydogenase complex
10 Coenzymes
NAD , NADP , FAD , NADH , NADPH , FADH 2
A = KCL
C = A / KL
C = 0.055 * 10 6 µ mol * Cm / 6.22 * 10 3 L * 1Cm
C = 0.055 * 10 6 µ mole * Cm / 6.22 * 10 3 103 ml * 1 Cm
No. of µmoles produced of NADH / min / vol. added of mitochondrial fraction
U/ml
U / g wet tissue
1M 3 -1 -1 E 1Cm for NADH ( NADPH ) at 340 nm = 6.22 * 10 L mol Cm
Zero time A = 0.726
1 min. = 0.772
2 min = 0826
3 min = 0.872
4 min = 0.934
5 min = 1.00
11 0.046
0.054
0.046
0.062
0.066
∆ A / min = 0.055
Some Lysosmal enzymes
12 Proteases ( for protein degradation )
Nucleases ( eg, ribonucleases , deoxyribonucleases )
Lipases ( for lipid degradation )
Galactosidases ( α – galactosidases , β- galactosidases )
Phosphatases ( for phosphate removal )
Lysosomal storage diseases ( LSD )
Cytosol fraction
18,000 rpm ( High speed centrifuge )
Marker : lactate dehydrogense LDH
Sod. Pyruvate + NADH + H + → lactate + NAD +
- + + - + CH3 C=O COO Na + NADH + H → CH3 CHOH COO + NAD
P → L
L → P
A = KCL
13 C = A / KL
C = 0.036 * 10 6 µ mol * Cm / 6.22 * 10 3 L * 1Cm
C = 0.036 * 10 6 µ mole * Cm / 6.22 * 10 3 103 ml * 1 Cm
No. of µmoles disappeared of NADH / min / vol. added of cytosolic fraction
U/ml
1 : 5 ( 1g / 5 ml )
1ml = 0.2 g
U / g wet tissue
1M 3 -1 -1 E 1Cm for NADH ( NADPH ) at 340 nm = 6.22 * 10 L mol Cm
Zero time A = 0.726
1 min. = 0.682
2 min = 0.640
3 min = 0.60
4 min = 0.31
5 min = 0.12
0.044
14 0.042
0.040
0.029
0.019
GOUT ( disorder of uric acid metabolism )
Cofactor
1. Coenzyme
2. Metal ion ( Mg , Zn , Ca …… etc )
15 3. Prosthetic group
Hydrophilic
Hydrophobic
GluT2
Hydrology
Microsomal & lysosomal fraction
Ultra centrifuge ( 75000 rpm )
Marker or indicator
Microsomal fraction
1. Glucose -6- phosphatase ( G6Pase )
G6p → Glucose + Phosphate ( Pi )
+6 Phosphate ( Pi ) +Ammonium molybdate → Phosphomolybdate ( Mo )
+3 + Reducing agent ( Vit.C : ascorbic acid ) → ( Mo ) Mo2O3
Molybdenum blue
Specificity
Mo : molybdenum
16 2. MFO : Mixed Function Oxidases ( drug metabolism )
Xenobiotics
Aldehyde oxidase
Xanthine oxidase
Lysosomal fraction
Indicator : Acid phosphatase ( ACP)
17 P- nitrophenyl phosphate → P-nitrophenol + Pi
Yellow in color
Λmax = 400 – 405 nm
Increase in A
Extinction coefficient = 18.7
Prostate cancer ( clinical application )
18