You are asked to measure the amount of β-glucosidase in a commercial enzyme solution containing 20 mg protein/mL of solution. You place 1 mL of this enzyme solution into 9 mL of an aqueous buffer solution containing 20 mM cellobiose. One unit of activity of β-glucosidase is defined as the amount of enzyme which produces 1 µmol of glucose per min in a 65 wt/v% solution of cellobiose at pH 5.0 and at 37°C. Initial rate experiments show that the reaction produces 1.8 µmol of glucose/mL.min. What is the specific activity of the commercial enzyme solution, in terms of # units/mg protein?
Unit of activity of β-glucosidase = amount enzyme / µmol of glucose per min
Unit of activity of β-glucosidase = 1mL of enzyme / 1.8 µmol of glucose per min
Unit of activity of β-glucosidase = 0.556 mL of enzyme/µmol of glucose per min = 0.556 units
Specific activity = 0.556 units / 20 mg protein
Specific activity = 0.0278 units / mg protein
You are asked to measure the amount of β-glucosidase in a commercial enzyme solution containing 20...
A crude cell extract containing 2 g.L -1 of protein was assayed for enzyme activity using an excess of substrate. It was found that 5 ml of the solution converted 25 µmoles of substrate to product over a period of 2 minutes. (i) Calculate the specific activity of the enzyme. The crude extract was subjected to anion exchange chromatography followed by gel filtration. After anion exchange the specific activity had risen to 226 µmoles.min-1 .mg-1 , and after gel filtration...
BADBO 23:22 601 < chapter-part2 Lipase can hydrolyze p- nitrophenolate ester to generate p- nitrophenol. Weigh 25mg lipase into 25ml buffer, take 2ml solution and measure the nitrogen is 0.2mg by Kjeldahl method. Take another 0.1 ml solution to measure the enzyme activity. As a result, p- nitrophenol ester was hydrolyzed to produce 15 mg p-nitrophenol per hour. One enzyme activity unit was defined as the amount of enzyme that produced 1 ug of p-nitrophenol per minute. Please calculate: (1)...
QUESTION THREE (20 MARKS) The enzyme malate dehydrogenase (MDIH) catalyses the following reaction: Malate +NADoxaloacetate + NADH a) Which of the six major groups of enzymes (oxidoreductases, transferases, hydrolases s] l lyases, isomerases and ligases) does MDH belong to? Explain your answer. 2 mark b) What equipment would you use to assay this reaction; what would you measure and why 14 Marks] c) Malate dehydrogenase from pig liver mitochondria has a K M of 0.3 mM malate. Sketch a graph...
PLEASE SHOW ALL WORK IF POSSIBLE! THANK YOU IN ADVANCE. 1) SOC media is 2% tryptone, 0.5% yeast extract, 10 mM NaCL (F.W. 58), 2.5 mM KCl (F.W. 74.5), 10 mM MgSO4 (F.W. 246.5), 10 mM MgCl2 (F.W. 203.3), 20 mM glucose (F.W. 180.16). Determine the amounts of each to make 500 mL of SOC. 2) Determine the number of moles in 0.05 μg of 300 bp insert DNA. There are 660 g/mol-bp. What is the molar ration of insert...
Based on the document below,
1. Describe the hypothesis Chaudhuri et al ids attempting to
evaluate; in other words, what is the goal of this paper? Why is he
writing it?
2. Does the data presented in the paper support the hypothesis
stated in the introduction? Explain.
3.According to Chaudhuri, what is the potential role of thew
alkaline phosphatase in the cleanup of industrial waste.
CHAUDHURI et al: KINETIC BEHAVIOUR OF CALF INTESTINAL ALP WITH PNPP 8.5, 9, 9.5, 10,...
lab question 1. What is the basis of the different purification methods? 2. What are some of the factors the might have interfered with your results? 3. How might you improve the process to increase the yield and purity? lab process E. coli BL21 (DE3) cells were transformed with the pET Topo-1521 vector containing a reading frame encoding the green fluorescent protein (GFP). Cells were cultured in M9ZB media at 37°C until the absorbance at 600 nm reached 0.7, at...
I need to write a conclusion for this lab. Based off these
results what kinds of conclusions can be drawn?
S OY Orre tes. A, B. Color, pH, Specific Gravity, and Electrolytes "Normal Urine Specimen" Test A. Color I clear "Abnormal Urine Specimen" slightly cloudy PH 2 1.10 gime! Specific gravity 0.70 glume - B. Electrolytes (Indicate absent - present +, strongly present ++) nornal Nat CI SO,2- PO,- 219 C-F. Glucose, Ketone Bodies, Protein, and Urobilinogen "Normal Urine Specimen"...
BELOW IS A METHOD. WHAT PROTOCOL (ALSO BELOW: A-F)
MATCHES THIS METHOD?
Method 5: Controlled ovarian stimulation and oocyte recovery was performed. Briefly, cycling females were subjected to follicular stimulation using twice-daily intramuscular injections of recombinant human FSH as well as concurrent treatment with Antide, a GnRH antagonist, for days 8-9. Unless indicated otherwise, all reagents were from Sigma-Aldrich and all hormones were from Ares Advanced Technologies Inc. Females received recombinant human luteinizing hormone on days 7-9 and recombinant...
Can you please explain in simple terms the methods of this experiment? I'm having difficulty visualizing and understanding what is being done. I have copied and pasted some of the text from the article. Thank you! Abstract : Obesity, high-fat diets, and subsequent type 2 diabetes (T2DM) are associated with cognitive impairment. Moreover, T2DM increases the risk of Alzheimer's disease (AD) and leads to abnormal elevation of brain beta-amyloid levels, one of the hallmarks of AD. The psychoactive alkaloid caffeine...
help please?
this was the only other information given
REPORT SHEET Determination of the Solubility-Product Constant for a Sparingly Soluble Salt EXPERIMENT 8 A. Preparation of a Calibration Curve Initial (Cro121 0.0024 M Absorbance 5 mL Volume of 0.0024 M K Cro Total volume 1. I mL 100 mL 2. 100ML 3. 10 mL 100ml 4. 15 mL 100 ML Molar extinction coefficient for [CrO2) [Cro,2) 2.4x100M 12x1044 2.4810M 3.6810M 0.04) 2037.37 0.85 1.13 2. 3. Average molar extinction coefficient...