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In‐Situ Atomic Force Microscopy Observation of Enzymatic Degradation in Poly(hydroxyalkanoic acid) Thin Films: Normal and Constrained Conditions
Author(s) -
Kikkawa Yoshihiro,
Hirota Takuya,
Numata Keiji,
Tsuge Takeharu,
Abe Hideki,
Iwata Tadahisa,
Doi Yoshiharu
Publication year - 2004
Publication title -
macromolecular bioscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.924
H-Index - 105
eISSN - 1616-5195
pISSN - 1616-5187
DOI - 10.1002/mabi.200300065
Subject(s) - lamellar structure , crystallization , materials science , crystal (programming language) , crystallography , thin film , chemical engineering , degradation (telecommunications) , chemistry , composite material , nanotechnology , telecommunications , computer science , engineering , programming language
Summary: The enzymatic degradation of lamellar crystals in poly(hydroxyalkanoic acid) thin films has been visualized by using in‐situ dynamic force mode (tapping mode) atomic force microscopy (AFM) in buffer solution. It was found that poly(hydroxybutyric acid) (PHB) depolymerase from Ralstonia pickettii T1 degraded the thin surface layers formed at room temperature first, and that lamellar crystals formed at the crystallization temperature (110 °C) were eroded from the crystallographic a ‐axis to show splintered morphologies at the tips of the crystals. In some cases, lamellar crystals were hydrolyzed from the crystallographic b ‐axis, resulting in the formation of small crevices. These results suggest that disordered molecular chain‐packing regions exist in the crystal along the crystallographic a ‐ and b ‐axes, and that enzymatic degradation predominantly occurs from these defective regions. In addition, cantilever‐tip‐induced enzymatic degradation was carried out in the presence of PHB depolymerase. A concave area was artificially formed on the stacked lamellar crystals by the AFM tip. In‐situ AFM observation has revealed that enzymatic degradation proceeds along both the longitudinal and lateral directions of the lamellae. At the same time, the PHB depolymerase preferentially eroded the concave area along the crystallographic c ‐axis. These results demonstrated that the PHB depolymerase predominantly degrades the less‐ordered molecular chain‐packing regions in the crystals.A series of AFM images of a poly{[( R )‐3‐hydroxybutyric acid]‐ co ‐[8‐mol%‐( R )‐3‐hydroxyhexanoic acid]} thin film during the cantilever‐tip‐induced enzymatic degradation process.