PGA (MW = 1.5–2.5 × 10
6) was purchased from Wako Pure Chemicals, Tokyo, Japan. Thermostable phosphorylase from
Aquifex aeolicus VF5 was supplied from Ezaki Glico Co. Ltd., Osaka, Japan.
19,43,44 (link) The primer-grafted PGA was synthesized according to the literature procedure.
38 (link)1H NMR (D
2O)
δ 1.86–2.01, 2.01–2.18 (br, β-CH
2 of PGA), 2.30–2.42 (br, γ-CH
2 of PGA), 3.40–4.08 (br, sugar protons of H2–H6), 4.12–4.25 (br, α-CH of PGA), 5.18, 5.41 (br s, H1 of primer). The DS for the grafting was determined by the integrated ratio of the H1 signal of the primer to the γ-CH
2 signal of PGA to be 70.2%. The guest polymer, PLLA, was synthesized by ring-opening polymerization of
l-lactide initiated with
l-lactic acid.
45 (link) The
Mn value was calculated by the integrated ratio of the main-chain signal to the terminal signal to be 1540. Other reagents and solvents were available commercially and used without further purification.
1H NMR spectra were recorded on JEOL
ECX400 spectrometer. XRD measurements were performed using a PANalytical
X'Pert Pro MPD diffractometer with Ni-filtered Cu Kα radiation (
λ = 0.15418 nm). UV-vis measurements were conducted using a Jasco
V-650Q1 spectrometer. The DLS measurements were obtained on a
Zetasizer Nano ZS (Malvern Instruments). IR spectra were recorded on a PerkinElmer
Spectrum Two spectrometer.
Kadokawa J.I., Orio S, & Yamamoto K. (2019). Formation of microparticles from amylose-grafted poly(γ-glutamic acid) networks obtained by thermostable phosphorylase-catalyzed enzymatic polymerization. RSC Advances, 9(28), 16176-16182.