PubMed · 6739333
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I Brook. Frontal sinusitis.. https://pubmed.ncbi.nlm.nih.gov/6739333/
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The purification of a thermostable Caldocellum saccharolyticum beta-glucosidase expressed in Escherichia coli was investigated using heat precipitation of unclarified cell homogenates. Heat treatment at 70 degrees C was capable of purification with respect to cell debris, small particulates and the majority of cell protein, although E. coli proteins were even more efficiently removed at 80 degrees C and above. For thermostable proteins expressed in E. coli, a precipitation temperature of 80 degrees C or greater is recommended for optimal removal of contaminant proteins. In small-scale heating trials, heating rate was found to influence enzyme yield significantly. Losses were minimised when 'flash-heating' was employed. The successful single-step removal of particulates, labile protein and nucleic acids was achieved by simultaneous heat-treatment and polyethyleneimine addition, although the purification achieved was additive rather than synergistic.
Mild acid hydrolysis of the smooth-type lipopolysaccharide (LPS) of Pectinatus frisingensis afforded no polysaccharide but monomeric 6-deoxy-L-altrose (L-6dAlt) which was identified by anion-exchange chromatography in borate buffer, GLC/MS, 1H-NMR spectroscopy, and optical rotation. LPS was degraded with alkali under reductive conditions to give a completely O-deacylated polysaccharide, which was studied by methylation analysis, 1H-NMR and 13C-NMR spectroscopy, including sequential, selective spin-decoupling, two-dimensional correlation spectroscopy (COSY), COSY with relayed coherence transfer, two-dimensional heteronuclear 13C, 1H-COSY, one-dimensional NOE and two-dimensional rotating-frame NOE spectroscopy. It was found that the O-specific polysaccharide chain of P. frisingensis LPS is a homopolymer of 6-deoxy-L-altrofuranose built up of tetrasaccharide-repeating units having the following structure: [sequence: see text] Similarly, mild acid degradation of smooth-type LPS of Pectinatus cerevisiiphilus resulted in depolymerisation of the polysaccharide chain to give a disaccharide consisting of D-glucose and D-fucose. Study of the disaccharide by methylation analysis and alkali-degraded LPS by one-dimensional and two-dimensional 1H-NMR and 13C-NMR spectroscopy showed that the O-specific polysaccharide of P. cerevisiiphilus has the following structure: -->2)-beta-D-Fucf-(1-->2)-alpha-D-Glcp-(1-->.
Biodegradability is one of the most important characteristics of an organic compound for predicting its fate and life in the environment and its application in biological wastewater treatment. But there is no general testing method for biodegradability under anaerobic conditions. The biodegradabilities of thirteen principal organic compounds was investigated in a batch test using vials under various conditions, such as the concentration of an organic compound, the cultivation method and the concentration of anaerobic bacteria for seeding. Two test methods in the standard concentration and the low concentration were developed. A new method to classify the biodegradabilities of organic compounds into thirteen ranks was proposed by considering inhibition, complete biodegradation and first step biodegradation.