ABSTRACT
Mucic acid is a hexaric acid that can be biosynthesized by oxidation of D-galacturonic acid, which is the main constituent of pectin. The structure and properties of mucic acid are similar to that of glucaric acid, and can be widely applied in the preparation of important platform compounds, polymers and macromolecular materials. Pectin is a cheap and abundant renewable biomass resource, thus developing a process enabling production of mucic acid from pectin would be of important economic value and environmental significance. This review summarized the structure and hydrolysis of pectin, the catabolism and regulation of D-galacturonic acid in microorganisms, and the strategy for mucic acid production based on engineering of corresponding pathways. The future application of mucic acid are prospected, and future directions for the preparation of mucic acid by biological method are also proposed.
Subject(s)
Hexuronic Acids/metabolism , Pectins/metabolism , Sugar Acids/metabolismABSTRACT
Objective: To compare the composition and content of polysaccharides in Polygonati Rhizoma by qualitative and quantitative analysis combined with chemometrics, and provide the reference for the quality evaluation of Polygonati Rhizoma. Methods Fourier transform infrared spectroscopy (FTIR) and pre-column derivatization-HPLC (PMP-HPLC) were employed to reveal the differences of polysaccharide among the three species, and the content of total polysaccharide was determined by ultraviolet spectroscopy (UV). Results:The result indicated that the average spectra and the second derivative atlas in FTIR fingerprint of Polygonati Rhizoma was significantly different. The PCA, PLS-DA and HCA analysis provided a further refinement of the method to distinguish three species. Furthermore, the PMP-HPLC showed that the components of monosaccharide and polysaccharides of three species were different. The main common components of the 10 common peaks were identified, which were as follows: D-mannose, D-ribose, L-rhamnose, D-galacturonic acid, D-glucuronic acid, D-galactose, D-glucose, D-xylose, D-arabinose and L-fucose. The content of the total polysaccharide meeted the requirements of Chinese pharmacopoeia 2015 edition Conclusion:The study provided a new reference for quality evaluation of P. Rhizoma.
ABSTRACT
OBJECTIVE:To establish a method for the content determination of saccharide in polysaccharides containing galact-uronic acid based on phenol-sulfuric acid method combined with correction factor method. METHODS:The determination condi-tion of phenol-sulfuric acid was optimized. A series of standard curves were drawn with glacturonic aid-glucose mixed control with different mass ratio. The content of saccharide in Codonopsis pilosula polysaccharides CPP1b samples containing galacturonic acid was determined. According to regression equation of galacturonic acid-glucose ratio of 0-100%,the correction factor was calculated by using C. pilosula polysaccharides CPP1b as the reference polysaccharide,and the results of content determination of saccharide were corrected. The rationality of this method was verified by using mixed monosaccharide control with same composition as C. pi-losula polysaccharides CPP1b. RESULTS:The correction factor of C. pilosula polysaccharide CPP1b to glucose was 3.33;in vali-dation test,the content of saccharide in mixed monosaccharide control with same composition as C. pilosula polysaccharides CPP1b was 103.47%. RSDs of precision and stability tests was <1%. The recoveries ranged 93.52%-107.35%(RSD=5.09%,n=6). CONCLUSIONS:The established method can accurately determine the content of saccharide in C. pilosula polysaccharides CPP1b containing galacturonic acid.
ABSTRACT
Introducción: la complejidad y diversidad estructural de los polisacáridos capsulares de Streptococcus pneumoniae hace que la metodología analítica necesaria para la caracterización y control de calidad sea engorrosa. El método colorimétrico mâhidroxibifenil desarrollado por Blumenkrantz y AsboeâHansen en el año 1973, permite contrarrestar las desventajas del método propuesto en la Farmacopea Europea 6ta Edición, 2011. Objetivo: validar el método mâhidroxibifenilo para cuantificar ácido urónico en polisacáridos purificados de streptococcus pneumoniae. Métodos: se determinó el tiempo de vigencia de la solución de tetraborato de sodio responsable de generar la respuesta analítica y se seleccionó una metodología para la cuantificación de ácido urónico por el método del mâhidroxibifenilo se emplea una solución estándar de ácido galacturónico a 1 mg/mL. Se realizó una evaluación de los parámetros de validación: linealidad, exactitud, precisión, rango y especificidad, según exigencias actuales. Además se comparó con el método del carbazol descrito en la Farmacopea Europea 6ta Edición, 2011 para la cuantificación de ácido urónico. Resultados: se demostró que el tiempo de vida útil de la solución de tetraborato de sodio fue de 24 h. El método del mâhidroxibifenilo fue específico, lineal, exacto y preciso en el rango de 2â20 µg/mL porque se cumplieron satisfactoriamente los criterios de aceptación establecidos para cada uno de ellos. La comparación del método propuesto con el método normalizado reveló que no existieron diferencias estadísticamente significativas entre ambos(AU) Conclusión: el método colorimétrico del mâhidroxibifenilo resultó válido para el control de calidad de las muestras de polisacárido purificado de Streptococcus pneumoniae, dando resultados comparables con el método recomendado en la Farmacopea Europea, 2011(AU)
Introduction: complexity and diversity in the structure of Streptococcus pneumoniae capsular makes the analytical methodology for characterization and quality control a troublesome aspect. The colorimetric m/hydroxibiphenil method devised by Blumenklrantz and Asboe-Hansen in 1973 allows reducing the disadvantages of the suggested method in the European Pharmacopea 6th edition, 2011. Objective: to validate the m-hydroxybiphenil method for quantitation of uronic acid in purified Streptococcus pneumonia polysaccharides. Methods: the length of validity of a sodium tetraborate solution, responsible for generating the analytical response, was estimated, and additionally, a methodology for quantitation of uronic acid by the m-hydroxybiphenil method was selected in which a standard galacturonic acid solution at 1mg/ml was used. The validation parameters were evaluated as follows: linearity, accuracy, precision, range and specificity, according to the present requirements. This method was compared with the carbazol method described in the European Pharmacopea 6th edition, 2011 for quantitation of uronic acid. Results: it was demonstrated that the useful lifetime of the sodium tetraborate solution was 24 hours. The m-hydroxybiphenil method was specific, linear, accurate and precise in the range of 2 to 20 ?g/mL because the set acceptance criteria were satisfactorily complied with for each of them. The comparison of the suggested method with the standardized method yielded that no statistically significant differences exist between them. Conclusions: the colorimetric m-hydroxybiphenil method proved to be valid for the quality control of purified Streptococcus pneumonia polysaccharide samples and the results are comparable to those of the recommended method in the European Pharmacopea, 2011(AU)