Objective: To track the chymotrypsin-catalyzed hydrolysis of p-nitrophenyl acetate using the spectrometers. Compound molecular FormulaMolecular WeightBoiling Point (°C) warming Point (°C)Density (g/cm3) p-nitrophenyl acetateC8H7NO4181.14--77-- acetonitrileC2H3N41.0582-450.786 Hydrochloric tartHCl36.46110-27.321.18 atomic number 11 phosphate dibasicNa2HPO4141.96--2500.5-1.2 Sodium phosphate monobasicNaH2PO4119.98------ chemic Structures p-nitrophenyl acetate acetonitrileHydrochloric AcidSodium phosphate dibasic Sodium orthophosphate monobasic Observations: For this lab, I was partnered up with 5 other people, should have been 3 but there were two extra in the class. First, we picked astonished 2 cuvettes to make sure they were free of chymotripsin. We left the decolourise in the cuvettes for roughly 1 hour, rinsed them with DI water for another minute, and rinsed them with propanone so that they dry without too much trouble. The weight I was charge was 15mg, the other weights were 5mg, 10mg, and 20mg. Once one cuvette was dry, we proceeded to make a zero for the spectrometer. We added 2 portions of 940uL of the phosphate wing and 100uL of p-nitrophenyl acetate. We utilise this insight to zero our spectrometer.
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Next, we each prepared our samples respectively and obtained the graph charge to our concentration of chymotrypsin. We used labtop 002, everything should be in the JABS folder. Data: clean Cuvettes term bleach left in cuvette~1 minute Time rinsed with DI water~1 minute Preparation of render Assigned weight15mg nitt y-gritty HCl in microcentrifuge tube1000uL ! total phosphate buffer in cuvette-940uL=1880uL total -940uL Amount p-nitrophenyl acetate in cuvette100uL Amount chymotrypsin solution used20uL Laptop 002JABS folder Conclusions: 1.What are the typical pKas of aspartate, histidine, and serine? a.The pKa of aspartate is 3.8 COOH speciate is 3.1 amine group is...If you want to get a adequate essay, order it on our website:
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