Synchrotron-based Fourier Transform Infrared Research Articles

The influence of phosphorus availability on carbon allocation and P quota in Scenedesmus subspicatus: A synchrotron-based FTIR analysis

D.C. Sigee, F. Bahrami, B. Estrada, R.E. Webster and A.P. Dean. 2007. The influence of phosphorus availability on carbon allocation and P quota in Scenedesmus subspicatus: A synchrotron-based FTIR analysis. Phycologia 46: 583–592. DOI: 10.2216/07-14.1Synchrotron-based Fourier transform infrared (FTIR) microspectroscopy was used to characterise the molecular composition of the freshwater alga Scenedesmus subspicatus, cultured at three different initial concentrations of phosphorus (PO4-P): 0.05 mg l−1, 0.5 mg l−1 and 5 mg l−1. These led, respectively, to limited algal growth due to phosphorus deficiency (low-P culture), maximum algal growth with no luxury consumption (intermediate-P) and maximum algal growth with luxury phosphorus consumption (high-P culture). In all cultures, FTIR spectra had nine major absorbance bands (wavenumber range 1760–900 cm−1), including bands at 1736 cm−1 (lipid), 1652 cm−1 (amide I) and the region from 1180 to 950 cm−1 (carbohydrate). Internal phosphorus concentrations (Qp), determined by energy dispersive X-ray microanalysis, differed markedly between low-P (typically < 0.1% dry wt), intermediate-P (> 0.1%) and high-P (> 0.3%) cultures. During logarithmic growth phase, a rapid change in carbon allocation was observed in the low-P cultures, with increases in both the lipid:protein (0.1–0.34) and carbohydrate:protein (0.4–1.0) ratio. Mean cell volume increased by 60%, and the mean chlorophyll a content remained consistently low (typically < 0.2 pg cell−1). The change in carbon allocation was triggered primarily by low Qp values rather than low external (culture medium) concentrations. Intermediate-P and high-P cultures showed higher chlorophyll a content (> 0.2 pg cell−1) and changes in carbon allocation only after entry into stationary phase. No increase in cell volume occurred, suggesting that a switch in carbon allocation during stationary phase (intermediate- and high-P cultures) rather than log phase (low-P culture) does not result in an increase in cell size. Entry into stationary growth phase occurred simultaneously in all three cultures and was not caused by internal (Qp) or external phosphorus depletion. Medium replacement in late stationary phase (day 35) cultures led to a rapid stimulation of growth, with a reversed carbon allocation (reduced lipid:protein and carbohydrate:protein ratios) and in low-P cultures a decrease in cell volume.

An emerging method for rapid characterization of feed structures and feed component matrix at a cellular leveland relation to feed quality and nutritive value

Feed quality, feed characteristics, nutrient utilization and digestive behaviour are closely related to: (i) total feed composition, (ii) feed intrinsic structures, and (iii) biological component matrix (such as protein to starch matrix, protein to carbohydrate matrix). Conventional “wet” chemical analysis can determine total chemical composition, but fails to detect the feed intrinsic structures and biological component matrix due to destruction of feed samples during the processing for chemical analysis and the “wet” chemical analysis cannot link structural information to chemical information within intact feed tissue. Recently, advanced synchrotron-based Fourier transform infrared (FTIR) microspectroscopy has been developed as a non-destructive and non-invasive structural-chemical analytical technique. This technique can link chemical information to structural information of biological samples within intact tissue within cellular dimensions. It can provide four kinds of information simultaneously: tissue composition, tissue structure, tissue chemistry and tissue environment. However, this novel technique has been found mainly for medical science research, extremely rare for feed science and nutrition research. The objective of this review article was to illustrate synchrotron-based FTIR microspectroscopy as a novel research tool for rapid characterization of feed structures at a cellular level and for detection of chemical features and molecular chemical make-up of feed biological component matrix and nutrient interaction. The emphasis of this article was to show that feed structural-chemical features at a cellular level are closely related to feed characteristics, feed quality and nutritive value in animals. The synchrotron-based technology will provide us with a greater understanding of the plant-animal interface.

Multicomponent Peak Modeling of Protein Secondary Structures: Comparison of Gaussian with Lorentzian Analytical Methods for Plant Feed and Seed Molecular Biology and Chemistry Research

The objective of this study was to compare Gaussian and Lorentzian multicomponent peak modeling methods in quantification of protein secondary structures of various plant seed and feed tissues within intact tissue at a cellular and subcellular level using the advanced synchrotron light sourced Fourier transform infrared (FT-IR) microspectroscopy (S-FTIR). This experiment was performed at the beamline U10B at the National Synchrotron Light Source (NSLS) in Brookhaven National Laboratory (BNL), U.S. Dept of Energy (NSLS-BNL, NY). The results show that in the comparison of the Gaussian and Lorentzian multi-peak modeling methods, the Gaussian method is more accurate for fitting multi-peak curves of protein secondary structures than the Lorentzian method, with higher modeling R(2) values (0.92 versus 0.89, P < 0.05). There were no large differences (P > 0.05) in the quantification of the relative percentage alpha-helices, beta-sheets, and others in protein secondary structures of the plant seed tissues, with averages of 30.2%, 40.4%, and 29.4%, respectively. However, there are significant differences (P < 0.05) in the quantification of the ratios of sheet alpha-helix (1.42 versus 1.60; SEM = 0.058) in protein secondary structures of the plant seed tissues. With synchrotron FT-IR microspectroscopy, the ultrastructural-chemical makeup and nutritive characteristics could be revealed at a high spatial resolution. Synchrotron-based FT-IR microspectroscopy revealed that the secondary structure of protein differed between the plant seed tissues in terms of relative percentage and ratio of protein secondary structures (alpha-helix and beta-sheet) within cellular dimensions. The results also show that the flaxseed tissues contained higher (P < 0.05) percentage alpha-helix (38.6 versus 24.0%) beta-sheet (45.3 versus 36.9%), lower (P < 0.05) percentage of other secondary structures (16.1% versus 39.0%), and higher (P < 0.05) ratios alpha-helix beta-sheet (0.90 versus 0.69) than the winterfat seed tissues. It must be mentioned that the relative percentages of protein secondary structure may not reflect the true secondary structure. However, the purpose of modeling the relative percentage of secondary structure was to detect the variety of differences among seed/feed/plant tissues and their relation to nutritive value and digestive behavior. The results demonstrate the potential of highly spatially resolved synchrotron-based FT-IR microspectroscopy to reveal protein secondary structures of the plant seed/feed tissues. Further study is needed to quantify the relationship between protein secondary structures and nutrient availability and digestive behavior of various varieties of plant seed tissues. Information from the infrared probing of protein secondary structures can be valuable as a guide to maintaining protein nutritive value and quality for animal and human use.

A study of cytokinetic and motile prostate cancer cells using synchrotron-based FTIR microspectroscopic imaging

Synchrotron-based Fourier transform infrared (SR-FTIR) microspectroscopy has been applied to the study of dynamic cellular events. SR-FTIR microspectroscopy is a powerful bioanalytical technique for the simultaneous analysis of proteins, lipids and a variety of phosphorylated molecules within whole cells. In this study, SR-FTIR microspectroscopy was used in imaging mode to generate biospectroscopic chemical maps of formalin-fixed PC-3 prostate cancer cells, which had been preserved in the process of cell division (cytokinesis) and locomotion. The distribution and intensity profiles of IR signals corresponding to the amide I and II (protein) and/or ν as and s (CH 3), ν as and s (CH 2) (lipid) modes were found to be useful in understanding fundamental biochemical processes at the midbody of the cytokinetic cells and at the lamellipodium of motile cells. Furthermore, in both of these cellular systems we observed a distinct hemispherical distribution of the lipid ester (C O) signal, which surrounded high phosphate signal. This feature was assigned to intracellular IR signals corresponding to membrane-rich organelles surrounding the cell nucleus.

Fixation protocols for subcellular imaging by synchrotron‐based Fourier transform infrared microspectroscopy

Synchrotron-based Fourier transform infrared (SR-FTIR) microspectroscopy is a powerful bioanalytical technique for the simultaneous analysis of lipids, proteins, carbohydrates, and a variety of phosphorylated molecules within intact cells. SR-FTIR microspectroscopy can be used in the imaging mode to generate biospectroscopic maps of the distribution and intensity profiles of subcellular biomolecular domains at diffraction-limited spatial resolution. However, the acquisition of highly spatially resolved IR images of cells is not only a function of instrumental parameters (source brightness, sampling aperture size) but also the cell preparation method employed. Additionally, for the IR data to be biochemically relevant the cells must be preserved in a life-like state without introducing artefacts. In the present study we demonstrate, for the first time, the differences in biomolecular localizations observed in SR-FTIR images of cells fixed by formalin, formalin-critical point drying (CPD), and glutaraldehyde-osmium tetroxide-CPD, using the PC-3 prostate cancer cell line. We compare these SR-FTIR images of fixed cells to unfixed cells. The influence of chemical fixatives on the IR spectrum is discussed in addition to the biological significance of the observed localizations. Our experiments reveal that formalin fixation at low concentration preserves lipid, phosphate, and protein components without significantly influencing the IR spectrum of the cell.

Using Synchrotron-Based FTIR Microspectroscopy To Reveal Chemical Features of Feather Protein Secondary Structure: Comparison with Other Feed Protein Sources

Studying the secondary structure of proteins leads to an understanding of the components that make up a whole protein. An understanding of the structure of the whole protein is often vital to understanding its digestive behavior in animals and nutritive quality. Usually protein secondary structures include alpha-helix and beta-sheet. The percentages of these two structures in protein secondary structures may influence feed protein quality and digestive behavior. Feathers are widely available as a potential protein supplement. They are very high in protein (84%), but the digestibility of the protein is very low (5%). The objective of this study was to use synchrotron-based Fourier transform infrared (FTIR) microspectroscopy to reveal chemical features of feather protein secondary structure within amide I at ultraspatial resolution (pixel size = 10 x 10 microm), in comparison with other protein sources from easily digested feeds such as barley, oat, and wheat tissue at endosperm regions (without destruction of their inherent structure). This experiment was performed at beamline U2B of the Albert Einstein Center for Synchrotron Biosciences at the National Synchrotron Light Source (NSLS) in Brookhaven National Laboratory (BNL), U.S. Dept of Energy (NSLS-BNL, Upton, NY). The results showed that ultraspatially resolved chemical imaging of feed protein secondary structure in terms of beta-sheet to alpha-helix peak height ratio by stepping in pixel-sized increments was obtained. Using synchrotron FTIR microspectroscopy can distinguish structures of protein amide I among the different feed protein sources. The results show that the secondary structure of feather protein differed from those of other feed protein sources in terms of the line-shape and position of amide I. The feather protein amide I peaked at approximately 1630 cm(-1). However, other feed protein sources showed a peak at approximately 1650 cm(-1). By using multicomponent peak modeling, the relatively quantitative amounts of alpha-helix and beta-sheet in protein secondary structure were obtained, which showed that feather contains 88% beta-sheet and 4% alpha-helix, barley contains 17% beta-sheet and 71% alpha-helix, oat contains 2% beta-sheet and 92% alpha-helix, and wheat contains 42% beta-sheet and 50% alpha-helix. The difference in percentage of protein secondary structure may be part of the reason for different feed protein digestive behaviors. These results demonstrate the potential of highly spatially resolved infrared microspectroscopy to reveal feed protein secondary structure. Information from this study by the infrared probing of feed protein secondary structure may be valuable as a guide for feed breeders to improve and maintain protein quality for animal use.

Imaging ToF-SIMS and synchrotron-based FT-IR microspectroscopic studies of prostate cancer cell lines

Imaging ToF-SIMS and synchrotron-based Fourier transform infrared (SR-FT-IR) microspectroscopy have been used to obtain chemical information from individual cells derived from human prostate cancer (CaP). ToF-SIMS imaging of molecular signals characteristic of membrane bound phospholipids are used to elucidate different fracture planes within individual freeze-fractured CaP cells. The localisation of Cu within the cytoplasm of cancer cells is consistent with increased metastatic potential. Line scans across CaP cells using SR-FT-IR microspectroscopy provide complimentary information on the localisation (±1 μm) of lipid and protein domains. This combined analytical approach offers a novel means of characterising individual CaP cells and investigating the biochemical basis of disease progression and metastases.

Molecular characterization of cyanobacterial silicification using synchrotron infrared micro-spectroscopy

Synchrotron-based Fourier-transform infrared (SR-FTIR) micro-spectroscopy was used to determine the concentration-dependent response of the organic structure of live cyanobacterial cells to silicification. Mid-infrared (4000–600 cm −1) measurements carried out on single filaments and sheaths of the cyanobacteria Calothrix sp. (strain KC97) were used to monitor the interaction between a polymerizing silica solution and the organic functional groups of the cells during progressive silicification. Spectra of whole-cells and sheaths were analyzed and the spectral features were assigned to specific functional groups related to the cell: lipids (-CH 2 and -CH 3; at 2870–2960 cm −1), fatty acids (>C=O at 1740 cm −1), proteins (amides I and II at 1650 and 1540 cm −1), nucleic acids (>P=O 1240 cm −1), carboxylic acids (C-O at 1392 cm −1), and polysaccharides (C-O between 1165 and 1030 cm −1). These vibrations and the characteristic vibrations for silica (Si-O between 1190 and 1060 cm −1; to some extent overlapping with the C-O frequencies of polysaccharides and Si-O at 800 cm −1) were used to follow the progress of silicification. Relative to unsilicified samples, the intensity of the combined C-O/Si-O vibration band increased considerably over the course of the silicification (whole-cells by > 90% and sheath by ∼75%). This increase is a consequence of (1) extensive growth of the sheath in response to the silicification, and (2) the formation of thin amorphous silica layers on the sheath. The formation of a silica specific band (∼800 cm −1) indicates, however, that the precipitation of amorphous silica is controlled by the dehydroxylation of abiotically formed silanol groups.