supported by the nsf plant genome research and reu programs *supported by the nsf plant genome...

Supported by the NSF Plant Genome

Research and REU Programs

*Supported by the NSF Plant Genome Research

and REU Programs

FTIR data analysis tutorial

Bryan Penning



Overview

• We are establishing infrared “spectrotypes” in cell wall mutants. Spectrotypes are spectroscopic phenotypes, i.e. the spectral differences between mutant and wild type populations.

• This tutorial will:– Give some background information on how we prepare and

collect data on mutants (See Techniques VII at: http://cellwall.genomics.purdue.edu/techniques/7.html for more details)

– Show how we analyze the data collected by Principal Components Analysis (PCA) and digital subtraction

– Give some example spectral peaks that indicate differences in cell wall composition between mutants and wildtype

http://cellwall.genomics.purdue.edu/techniques/7.html



Plant preparation• All plants are grown and cell walls isolated under the

same conditions and processed simultaneously for internal consistency of mutant and wild type comparisons (see Techniques VII for greater detail: http://cellwall.genomics.purdue.edu/techniques/7.html)– Wild type plants are always prepared with mutant plants– Plants are all grown on one-half strength MS salts with 1%

sucrose and 0.8% agar in the light for 12 days– Plants are all transferred to the dark for 2 days to lower

starch content (a contaminating feature in IR spectrum)– Plant tissue is crushed in liquid nitrogen, and non cell wall

components, such as proteins, are extracted using an SDS-Tris buffer

– Cell walls are isolated by homogenization in a Geno-Grinder (SPEX Certi-Prep), collected on a nylon mesh and washed with water and ethanol

– Cell walls are resuspended in distilled water and spotted on a gold-plated slide (EZ-Spot, Spectra-Tech) for spectral acquisition in an FTIR spectrometer (Thermo-Electron, Madison, WI )

http://cellwall.genomics.purdue.edu/techniques/7.html



FTIR spectral acquisition

• Spectra are acquired in a range of 4000 to 650 cm–1; 1 spectrum consists of 128 co-added scans with an eight- wavenumber resolution

• The following spectral characteristics are used to ensure that readings can be compared:– 0.4 to 0.8 max peak reading @ 1050-1000 cm-1

– Peak @ 1050-1000 cm-1 greater than peak @ 1600 cm-1

– The values @ 1800 cm-1 and 800 cm-1 are fairly equal with a value below 0.3 absorbance (to ensure a good baseline correction)

– Noisy spectra are discarded



FTIR data analysis

• Fig. A: We collect many spectra (about 40) with a computer driven stage and Omnic software (Thermo Electron), saving them as grouped data (*.spa)

• Fig. B: We convert group data to individual *.jdx files in Omnic

A

B



FTIR data analysis

•With the DOS command, RENAME, we convert *.jdx files into *.dx files that Win-Das software can recognize

•We use Win-Das (Kemsley, 1998)* software to analyze our data instead of Omnic because it is capable of area averaging the spectra, an essential feature of spectral analysis of plant cell walls because the samples vary in thickness

* Kemsley. 1998. Discriminant Analysis of Spectroscopic Data. Chichester, UK: John Wiley and Sons



FTIR data analysis• In Win-Das we first construct a

matrix• We add all of our spectra

(observations)• We view the spectra



FTIR data analysis• In Win-Das we:

– Truncate the spectra from 1801.2 to 798.4 cm-1 (useful wavenumber range for cell wall molecules)

– Baseline correct the spectra – Normalize the spectra and save as a

.txt (spectra) or .wdd (analysis) file



FTIR data analysis• Saving data for the web

– After normalizing we save the file as CF-Text (column-wise)

– This generates a *.txt file we copy and paste into Excel



FTIR data analysis

• You can download these spectra from our website (Families Tables)

• You can average the spectra using the average command in Excel



FTIR data analysis• Digital subtraction

– To perform a digital subtraction, average the mutant and wild-type spectra (previous slide) and copy over the spectra values (left column of spectra files)

– Subtract mutant from wild type and plot versus wavenumber (cm-1)

– Look for peaks (differences in cell wall components)



FTIR data analysis• Absorbances of specific peaks in the IR spectrum can be

correlated with particular cell wall molecules (Kačuráková et al, 2000)*:– Cellulose: 1162, 1120, 1059, 1033, 930, and 898 cm-1

– Pectin: 1144, 1100, 1047, 1017, 953, 896 cm-1

– Rhamnogalacturonan: 1150, 1122, 1070, 1043, 989, 951, 916, 902 cm-1

– Xyloglucan: 1153, 1118, 1078, 1041, 945, 897 cm-1

• However, these peak assignments are based on isolated polysaccharides and peaks may shift depending on molecular interactions and environment within the cell wall

• The more peaks that can be assigned to a particular polymer, the more likely that component differs between mutant and wild type cell walls

* Kačuráková, Capek, Sasinková, Wellner, and Ebringerová. 2000. FT-IR study of plant cell wall model compounds: pectic polysaccharides and hemicelluloses. Carbohydrate Polymers 43:195- 203



FTIR data analysis

• To develop Discriminant Analysis for our classifications (PCAs) in Win-Das– We create two groups (one wild type

and one mutant)– We compress the data using the

covariance method



FTIR data analysis• PCA analysis:

– Cluster plot of separation by PCAs– Loading plots (difference in groups)

• Discriminate– We use Squared Mahalanobis

distance to see number of correct classifications



FTIR data analysis

• PCA from Variance scores are shown in the gene family table…– Number of Principal Components

(PCs)– Percent classified (75/80 = 93%)

supported by the nsf plant genome research and reu programs *supported by the nsf plant genome...

Documents

nsf plant genome research

reu programs plant preparation

b slide

grouped data

group data

mutant plants plants

wi slide

wildtype slide