How does the substrate concentration affect the speed of enzymatic reactions?
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What are the favorable conditions for formation of Anions?
What factors contribute to the entropy change when a denatured protein folds up?
Explain who proposed law of mass action? What does it states?
Which is the most stable sulphur at room temperature?
if hydrogen ion concentration of a solution is 90% what will be the ph of that solution?
What types of things happen to proteins during posttranslational processing (hydroxylation, etc.)?
what are the reasons for gaucher's disease?
What is the difference between myoglobin and haemoglobin in the sequence of poly peptides?
How the pure culture can be produced?
southern blot technique is related to--------- [fill the gaps]
Which cellular compartment becomes acidic during mitochondrial electron transport?
I have given the protocol for the cyclodextrin glygosyl transferase assay: One ml of appropriately diluted enzyme sample was incubated at 60 °C for 15 min with 5 ml of 1% (w/v) gelatinized soluble starch in 50 mM, 7.0-pH Tris–HCl buffer. Reaction was terminated by boiling the reaction mixture for 3 min and reaction volume was made to 10 ml with distilled water. Two ml of above reaction mixture was withdrawn and mixed with 3 ml of Tris–HCl buffer, 5 ml of 125 mM Na2CO3, and 0.5 ml of phenolphthalein (25 mg phenolphthalein/100 ml absolute alcohol). Absorbance was measured at 550 nm. The percent decrease of sample was calculated with respect to control containing 5 ml of buffer, 5 ml of sodium carbonate and 0.5 ml of phenolphthalein. where Acontrol = absorbance of control and Atest = absorbance of sample. The amount of β-cyclodextrin (β-CD) produced was estimated from the standard graph of 0–500 μg/ml β-CD concentration against % decrease in absorbance. One unit of CGTase was defined as the amount of enzyme required to produce 1 μm of β-CD/min. Please can you suggest me the formula for the defination given in the last line