R Dataset / Package datasets / Puromycin

How To Create a Barplot

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How To Create a Stacked Barplot

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How To Create a Pie Chart

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How To Compute the Mean

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How To Create a Plot

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How to Compute the Median

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Boxplot

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Correlation Coefficient

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Cumulative Frequency Histogram

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Dotplot

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Hollow Histogram

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Numerical Summaries

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Pie Chart

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Plot

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Regression

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Stem and Leaf Plots

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Visual Summaries

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Submitted by pmagunia on March 9, 2018 - 1:06 PM
<iframe src="https://embed.picostat.com/r-dataset-package-datasets-puromycin.html" frameBorder="0" width="100%" height="307px" />
Attachment Size
dataset-22769.csv 470 bytes
Dataset License
GNU General Public License v2.0
Documentation License
GNU General Public License v2.0
Documentation

On this Picostat.com statistics page, you will find information about the Puromycin data set which pertains to Reaction Velocity of an Enzymatic Reaction. The Puromycin data set is found in the datasets R package. You can load the Puromycin data set in R by issuing the following command at the console data("Puromycin"). This will load the data into a variable called Puromycin. If R says the Puromycin data set is not found, you can try installing the package by issuing this command install.packages("datasets") and then attempt to reload the data. If you need to download R, you can go to the R project website. You can download a CSV (comma separated values) version of the Puromycin R data set. The size of this file is about 470 bytes.


Reaction Velocity of an Enzymatic Reaction

Description

The Puromycin data frame has 23 rows and 3 columns of the reaction velocity versus substrate concentration in an enzymatic reaction involving untreated cells or cells treated with Puromycin.

Usage

Puromycin

Format

This data frame contains the following columns:

conc

a numeric vector of substrate concentrations (ppm)

rate

a numeric vector of instantaneous reaction rates (counts/min/min)

state

a factor with levels treated untreated

Details

Data on the velocity of an enzymatic reaction were obtained by Treloar (1974). The number of counts per minute of radioactive product from the reaction was measured as a function of substrate concentration in parts per million (ppm) and from these counts the initial rate (or velocity) of the reaction was calculated (counts/min/min). The experiment was conducted once with the enzyme treated with Puromycin, and once with the enzyme untreated.

Source

Bates, D.M. and Watts, D.G. (1988), Nonlinear Regression Analysis and Its Applications, Wiley, Appendix A1.3.

Treloar, M. A. (1974), Effects of Puromycin on Galactosyltransferase in Golgi Membranes, M.Sc. Thesis, U. of Toronto.

See Also

SSmicmen for other models fitted to this dataset.

Examples

require(stats); require(graphics)plot(rate ~ conc, data = Puromycin, las = 1,
     xlab = "Substrate concentration (ppm)",
     ylab = "Reaction velocity (counts/min/min)",
     pch = as.integer(Puromycin$state),
     col = as.integer(Puromycin$state),
     main = "Puromycin data and fitted Michaelis-Menten curves")
## simplest form of fitting the Michaelis-Menten model to these data
fm1 <- nls(rate ~ Vm * conc/(K + conc), data = Puromycin,
           subset = state == "treated",
           start = c(Vm = 200, K = 0.05))
fm2 <- nls(rate ~ Vm * conc/(K + conc), data = Puromycin,
           subset = state == "untreated",
           start = c(Vm = 160, K = 0.05))
summary(fm1)
summary(fm2)
## add fitted lines to the plot
conc <- seq(0, 1.2, length.out = 101)
lines(conc, predict(fm1, list(conc = conc)), lty = 1, col = 1)
lines(conc, predict(fm2, list(conc = conc)), lty = 2, col = 2)
legend(0.8, 120, levels(Puromycin$state),
       col = 1:2, lty = 1:2, pch = 1:2)## using partial linearity
fm3 <- nls(rate ~ conc/(K + conc), data = Puromycin,
           subset = state == "treated", start = c(K = 0.05),
           algorithm = "plinear")

--

Dataset imported from https://www.r-project.org.
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