Bacterial Poly (bacterial + poly)

Distribution by Scientific Domains


Selected Abstracts


Biodegradable Water Absorbent Synthesized from Bacterial Poly(amino acid)s

MACROMOLECULAR BIOSCIENCE, Issue 3 2004
Masao Kunioka
Abstract Summary: Biodegradable hydrogels prepared by , -irradiation from microbial poly(amino acid)s have been studied. pH-Sensitive hydrogels were prepared by the , -irradiation of poly(, -glutamic acid) (PGA) produced by Bacillus subtilis and poly(, -lysine) (PL) produced by Streptomyces albulus in aqueous solutions. When the , -irradiation dose was 19 kGy or more, and the concentration of PGA in water was 2 wt.-% or more, transparent hydrogels could be produced. For the 19 kGy dose, the produced hydrogel was very weak, however, the specific water content (wt. of absorbed water/wt. of dry hydrogel) of this PGA hydrogel was approximately 3,500. The specific water content decreased to 200, increasing when the , -irradiation dose was over 100 kGy. Under acid conditions or upon the addition of electrolytes, the PGA hydrogels shrunk. The PGA hydrogel was pH-sensitive and the change in the volume of the hydrogel depended on the pH value outside the hydrogel in the swelling medium. This PGA hydrogel was hydrodegradable and biodegradable. A new novel purifier reagent (coagulant), made from the PGA hydrogels, for contaminated turbid water has been found and developed by Japanese companies. A very small amount of this coagulant (only 2 ppm in turbid water) with poly(aluminum chloride) can be used for the purification of turbid water. A PL aqueous solution also can change into a hydrogel by , -irradiation. The specific water content of the PL hyrdogel ranged from 20 to 160 depending on the preparation conditions. Under acid conditions, the PL hydrogel swelled because of the ionic repulsion of the protonated amino groups in the PL molecules. The rate of enzymatic degradation of the respective PL hydrogels by a neutral protease was much faster than the rate of simple hydrolytic degradation. [source]


Shape Memory Effect of Bacterial Poly[(3-hydroxybutyrate)- co -(3-hydroxyvalerate)],

MACROMOLECULAR RAPID COMMUNICATIONS, Issue 13 2005
Young Baek Kim
Abstract Summary: A bacterial poly[(3-hydroxybutyrate)- co -(3-hydroxyvalerate)] biosynthesized by Pseudomonas sp. HJ-2 was found to be a shape memory polymer. Permanent shapes were set by annealing at room temperature the samples that had been pre-treated above 95,°C in specified shapes. The temporary shapes were set by stretching and holding the elongated samples. Thermal shrinkage began at 45,°C and stopped at 75,°C to recover to their permanent shapes. Apparently, the orientation induced the formation of hard segments that were responsible for setting the temporary shapes. The shape memory effect of this polymer was explained based on the DSC and XRD results at different phases. The recovery of a coil shape upon heating a strip of HJ-2 PHB35V, demonstrating the polymers shape memory effect. [source]


A simple HPLC-MS method for the quantitative determination of the composition of bacterial medium chain-length polyhydroxyalkanoates

JOURNAL OF SEPARATION SCIENCE, JSS, Issue 10 2008
Andreas Grubelnik
Abstract Bacterial poly(hydroxyalkanoates) (PHAs) vary in the composition of their monomeric units. Besides saturated side-chains, unsaturated ones can also be found. The latter leads to unwanted by-products (THF ester, secondary alcohols) during acidic cleavage of the polymer backbone in the conventional analytical assays. To prevent these problems, we developed a new method for the reductive depolymerization of medium chain-length PHAs, leading to monomeric diols that can be separated and quantified by HPLC/MS. Reduction is performed at room temperature with lithium aluminum hydride within 5,15 min. The new method is faster and simpler than the previous ones and is quantitative. The results are consistent with the ones obtained by quantitative 1H NMR. [source]


Graft copolymers of methyl methacrylate and poly([R]-3-hydroxybutyrate) macromonomers as candidates for inclusion in acrylic bone cement formulations: Compression testing

JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2006
Sophie Nguyen
Abstract Graft copolymers of methyl methacrylate and biodegradable, biocompatible bacterial poly([R]-3-hydroxybutyrate) (PHB) blocks were synthesized and evaluated as possible constituents in acrylic bone cements for use in orthopaedic applications. The copolymers were produced by conventional free radical copolymerization and incorporated in one commercially available acrylic bone cement brand, Antibiotic Simplex® (AKZ). Cements with formulations containing 6.7 and 13.5 wt % of PMMA- graft -PHB were prepared. The morphology of the graft copolymer particles was suggested to influence the ability of the modified cement to be processed. Formulations containing more than about 20 wt % of the graft copolymer resulted in cement doughs that, both after first preparation and several hours later, were either sandy or soft spongy in texture and, thus, would be unacceptable for use in orthopaedic applications. The morphologies of the powders and the volumetric porosity (p) and ultimate compressive strength (UCS) of the cured cements were determined. Micro computed tomography showed that the cements presented average porosities of 13.5,16.9%. It was found that, while the powder particle shape and size for the experimental cements were markedly different from those of AKZ, there was no significant difference in either p or UCS for these cements. The latter was determined to be about 85 MPa for the modified cements and 84 MPa for Antibiotic Simplex. Furthermore, the UCS of all the cements exceeded the minimum level for acrylic bone cements, as stipulated by ASTM F-451. © 2005 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2006 [source]


Miscibility and Physical Properties of Poly(3-hydroxybutyrate -co- 3-hydroxyhexanoate)/Poly(ethylene oxide) Binary Blends

MACROMOLECULAR MATERIALS & ENGINEERING, Issue 12 2009
Fang Yu
Abstract In order to improve some inferior physical properties of bacterial poly(3-hydroxybutyrate -co- 3-hydroxyhexanoate) [P(3HB -co- 3HHx)] by blending with PEO, the miscibility, spherulite morphology, crystallization behavior and mechanical properties of P(3HB -co- 3HHx)/PEO binary biodegradable polymer blends were investigated. A good miscibility between P(3HB -co- 3HHx) with a 3HHx unit content of 11 mol-% and PEO in the amorphous state was found when the PEO weight fraction was 10,wt.-%, while the miscibility decreased dramatically when the PEO weight fraction exceeded 20,wt.-%. Strongly depending on the blend composition, the mechanical properties of P(3HB -co- 3HHx) was found to be significantly improved by blending with PEO with a weight fraction of ,5,17.5,wt.-%. [source]


Shape Memory Effect of Bacterial Poly[(3-hydroxybutyrate)- co -(3-hydroxyvalerate)],

MACROMOLECULAR RAPID COMMUNICATIONS, Issue 13 2005
Young Baek Kim
Abstract Summary: A bacterial poly[(3-hydroxybutyrate)- co -(3-hydroxyvalerate)] biosynthesized by Pseudomonas sp. HJ-2 was found to be a shape memory polymer. Permanent shapes were set by annealing at room temperature the samples that had been pre-treated above 95,°C in specified shapes. The temporary shapes were set by stretching and holding the elongated samples. Thermal shrinkage began at 45,°C and stopped at 75,°C to recover to their permanent shapes. Apparently, the orientation induced the formation of hard segments that were responsible for setting the temporary shapes. The shape memory effect of this polymer was explained based on the DSC and XRD results at different phases. The recovery of a coil shape upon heating a strip of HJ-2 PHB35V, demonstrating the polymers shape memory effect. [source]


A Physical Method of Fabricating Hollow Polymer Spheres Directly from Oil/Water Emulsions of Solutions of Polymers,

MACROMOLECULAR RAPID COMMUNICATIONS, Issue 18 2004
Young Baek Kim
Abstract Summary: A new physical method of fabricating hollow spheres from different polymers has been developed. In this method, emulsions were prepared by mixing organic solutions of polystyrene, poly(D,L -lactide- co -glycolide) (PLGA), and bacterial poly(3-hydroxybutyrate- co -3-hydroxyvalerate) (PHBV), water, and surfactants. The evaporation of solvents at room temperature caused a phase separation that eventually yielded hollow spheres. Molecular weights, concentrations of polymers, and the natures of surfactant and solvent were important aspects of hollow sphere formation and structure. A mechanism for the formation of hollow spheres is proposed based on observations made using an optical microscope equipped with a digital camcorder and using scanning electron microscopy images of hollow spheres obtained under different conditions. A scanning electron microscopy image of a broken smaller hollow sphere prepared using a 7 wt.-% polystyrene solution (diameter of the sphere ,10 micrometers). [source]


Electrospray ion-trap multistage mass spectrometry for characterisation of co-monomer compositional distribution of bacterial poly(3-hydroxybutyrate- co -3-hydroxyhexanoate) at the molecular level

RAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 20 2003
yna Adamus
We report an electrospray ionisation multistage mass spectrometry (ESI-MSn) method that utilises molecular mass information for determination of sequence distribution and chemical structure of mass-selected macromolecules of poly(3-hydroxybutyrate- co -3-hydroxyhexanoate) biopolyester, PHBH. On the basis of ESI-MSn studies of PHBH oligomers obtained by partial alkaline depolymerisation of natural PHBH containing 13,14,mol% of hydroxyhexanoate (HH) units, the microstructure of this bacterial copolyester was assessed up to the level of 28 repeat units. The subtle structural details of the PHBH were evaluated based on sequencing of individual macromolecular ions thus showing the utility of this technique for the analysis of biological copolyester macromolecules. It was confirmed that both HH and hydroxybutyrate (HB) units of the PHBH copolymer are randomly distributed. Copyright © 2003 John Wiley & Sons, Ltd. [source]