You contact an academic lab that specializes in synthesizing boronic acid analogs that have been shown to act as reversible inhibitors of the AmpC B-lactamase from Escherichia coll. The lab agrees to...


Based on your Lineweaver-Burk plot, what is the mode of PaESBL-1 inhibition by NSAMB?


What is the equation for the double-reciprocal plot at 20 nMnM NAMB?


You contact an academic lab that specializes in synthesizing boronic acid analogs that have been shown to act as reversible inhibitors of the AmpC B-lactamase from Escherichia coll. The lab agrees to send you several of its compounds to test against PAESBL-1. You begin by<br>looking at the potential of (napthylmethanesulfonylamino)methaneboronic acid (NSAMB) to inhibit the P. aeruginosa B-lactamase:<br>он<br>B<br>O=S- NH<br>OH<br>NSAMB<br>You perform a classic reversible inhibition experiment, where you measure the initial velocity for a range of substrate and inhibitor concentrations. For this assay, you use the artificial chromogenic substrate, CENTA:<br>`NO<br>CENTA<br>CENTA is hydrolyzed by B-lactamases to yield a product with absorbance at 405 nm.<br>The results of your experiment are listed in the table:<br>Initial velocity measurements (mAbs/s)<br>CENTA concentration<br>(µM)<br>[NSAMB) = 0 nM<br>[NSAMB) = 20 nM<br>[NSAMB] = 40 nM<br>[NSAMB) = 80 nM<br>15<br>0.125<br>0.102<br>0.087<br>0.066<br>30<br>0.167<br>0.145<br>0.129<br>0.105<br>60<br>0.200<br>0.184<br>0.170<br>0.148<br>120<br>0.222<br>0.212<br>0.202<br>0.186<br>240<br>0.235<br>0.229<br>0.224<br>0.213<br>

Extracted text: You contact an academic lab that specializes in synthesizing boronic acid analogs that have been shown to act as reversible inhibitors of the AmpC B-lactamase from Escherichia coll. The lab agrees to send you several of its compounds to test against PAESBL-1. You begin by looking at the potential of (napthylmethanesulfonylamino)methaneboronic acid (NSAMB) to inhibit the P. aeruginosa B-lactamase: он B O=S- NH OH NSAMB You perform a classic reversible inhibition experiment, where you measure the initial velocity for a range of substrate and inhibitor concentrations. For this assay, you use the artificial chromogenic substrate, CENTA: `NO CENTA CENTA is hydrolyzed by B-lactamases to yield a product with absorbance at 405 nm. The results of your experiment are listed in the table: Initial velocity measurements (mAbs/s) CENTA concentration (µM) [NSAMB) = 0 nM [NSAMB) = 20 nM [NSAMB] = 40 nM [NSAMB) = 80 nM 15 0.125 0.102 0.087 0.066 30 0.167 0.145 0.129 0.105 60 0.200 0.184 0.170 0.148 120 0.222 0.212 0.202 0.186 240 0.235 0.229 0.224 0.213

Jun 10, 2022
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