Enzymatic Degradation Processes of Lamellar Crystals in Thin Films for Poly[(R)-3-hydroxybutyric acid] and Its Copolymers Revealed by Real-Time Atomic Force Microscopy
| Autor: | Keiji Numata, Yoshihiro Kikkawa, Yoshiharu Doi, Hideki Abe, Tadahisa Iwata, Takeharu Tsuge, Takuya Hirota |
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| Rok vydání: | 2004 |
| Předmět: |
Reaction mechanism
Time Factors Materials science Polymers and Plastics Macromolecular Substances Polymers Polyesters Kinetics Biophysics Hydroxybutyrates Bioengineering Ralstonia Crystallography X-Ray Microscopy Atomic Force Biophysical Phenomena Biomaterials Crystal chemistry.chemical_compound X-Ray Diffraction Polymer chemistry Materials Chemistry Copolymer Scattering Radiation Lamellar structure Thin film X-Rays Comonomer Temperature Enzymes Polyester Crystallography chemistry Crystallization Carboxylic Ester Hydrolases |
| Zdroj: | Biomacromolecules. 5:2186-2194 |
| ISSN: | 1526-4602 1525-7797 |
| DOI: | 10.1021/bm0497670 |
| Popis: | Enzymatic degradation processes of flat-on lamellar crystals in melt-crystallized thin films of poly[(R)-3-hydroxybutyric acid] (P(3HB)) and its copolymers were characterized by real-time atomic force microscopy (AFM) in a phosphate buffer solution containing PHB depolymerase from Ralstonia pickettii T1. Fiberlike crystals with regular intervals were generated along the crystallographic a axis at the end of lamellar crystals during the enzymatic degradation. The morphologies and sizes of the fiberlike crystals were markedly dependent on the compositions of comonomer units in the polyesters. Length, width, interval, and thickness of the fiberlike crystals after the enzymatic degradation for 2 h were measured by AFM, and the dimensions were related to the solid-state structures of P(3HB) and its copolymers. The width and thickness decreased at the tip of fiberlike crystals, indicating that the enzymatic degradation of crystals takes place not only along the a axis but also along the b and c axes. These results from AFM measurement were compared with the data on crystal size by wide-angle X-ray diffraction, and on lamellar thickness and long period by small-angle X-ray scattering. In addition, the enzymatic erosion rate of flat-on lamellar crystals along the a axis was measured from real-time AFM height images. A schematic glacier model for the enzymatic degradation of flat-on lamellar crystals of P(3HB) by PHB depolymerase has been proposed on the basis of the AFM observations. |
| Databáze: | OpenAIRE |
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