ABSTRACT
This study was conducted to classify petroleum oils in terms of their biodegradation stage by using spectroscopic analysis associated to chemometric treatments. Principal Component Analysis (PCA) has been applied on infrared and UV fluorescence spectra of Brazilian and Pyrenean oils. For Brazil samples, the method allowed to distinguish the biodegraded oils from the non-affected ones. Pyrenean sampling including oils at different levels of biodegradation has been chosen to follow their alteration rate. PCA loadings have shown spectral regions which have differentiated oils after biodegradation whereas Simple-to-use Interactive Self-Modelling Mixture Analysis (SIMPLISMA) has permitted to obtain a repartition in terms of components families (saturated, aromatic and polar ones) characterizing chemical composition of oils at different biodegradation degrees. Results are in good agreement with conclusions of usual hydrocarbon biomarker analysis.
Subject(s)
Fuel Oils/analysis , Spectrum Analysis/methods , Brazil , Complex Mixtures/chemistry , Europe , Fluorescence , Fuel Oils/microbiology , Gas Chromatography-Mass Spectrometry , Principal Component Analysis , Reproducibility of Results , Spectroscopy, Fourier Transform InfraredABSTRACT
Hb Montefiore was found, in the heterozygous state, in a Puerto Rican female who had a slightly elevated total Hb level. Structural analysis revealed that Asp-alpha126 was replaced by Tyr. Hb Montefiore migrates close to HbF (at pH 8.6) and accounts for 20.3% of the hemolysate. Oxygen binding of red blood cells revealed a 40% decrease in the P50 (pH 7.4) and a low n value of 1.6 (normal: 2.6). Depletion of red blood cell 2,3-DPG did not change the results. Stripped Hb Montefiore at pH 7.2 showed an 8-fold reduction in P50 (0.6 versus 4.6 mm Hg) and very low cooperativity (n = 1.2 versus 2.9 for the control). Heterotopic effectors, as 2,3-diphosphoglycerate and inositol hexaphosphate had a normal effect and in addition, they increased cooperativity. The chloride ion effect and the Bohr effect were moderately reduced. A bezafibrate derivative (L345), known to bind alpha126, increases the P50 of HbA by 9-fold, but only by 1. 5-fold that of Hb Montefiore. Combining these functional studies with intrinsic fluorescence and Resonance Raman spectroscopy, we interpret the very low n value and the high oxygen affinity for Hb Montefiore as a result of both a destabilized T state that switches to R upon ligand binding and a deoxy T state that binds ligands with higher affinity than that of deoxy HbA. Hb Montefiore still binds ligands cooperatively, but the difference in ligand binding properties of the two quaternary states has been drastically reduced.
Subject(s)
Hemoglobins, Abnormal/chemistry , Hemoglobins, Abnormal/genetics , Hemoglobins, Abnormal/metabolism , Mutation , Oxygen/metabolism , Allosteric Regulation , Aspartic Acid/genetics , Chromatography, High Pressure Liquid , Erythrocytes/metabolism , Female , Heterozygote , Humans , Infant, Newborn , Puerto Rico/ethnology , Spectrometry, Fluorescence , Spectrum Analysis, Raman , Tyrosine/geneticsABSTRACT
Hb J-Cordoba [alpha 2A beta 2(95)(FG2)Lys----Met], is one of the few hemoglobin variants discovered in Argentina. The structure and functional abnormalities are described. Hb J-Cordoba exhibits a slightly increased oxygen affinity, low cooperativity, and normal interaction with heterotropic cofactors.