葡萄糖酸
葡萄糖氧化酶
化学
共价键
羧甲基纤维素
纤维素酶
有机化学
固定化酶
纤维素
催化作用
氧化物
核化学
生物传感器
酶
基质(水族馆)
戊二醛
化学工程
作者
Han Zhang,Shaofeng Hua,Lei Zhang
摘要
Abstract BACKGROUND The objective of this research was to use a step‐by‐step method to prepare a novel biocatalytic system (GO‐CEL‐E/N‐GA‐GOD): ‐OH and ‐COOH on the surface of graphene oxide (GO) were used to immobilize cellulase (CEL) and glucose oxidase (GOD), respectively, which may be easier to control the loading of enzymes with different kinds, to achieve the one‐pot conversion of gluconic acid from carboxymethyl cellulose (CMC). RESULTS The loadings capability of CEL and GOD on GO‐CEL‐E/N‐GA‐GOD were 49.07 ± 7.47 mg g−1 and 10.22 ± 2.03 mg g−1, respectively. The multi‐enzyme systems had shallow temperature and pH optima of 40 °C and 5.0. The kinetic constants of GO‐CEL‐E/N‐GA‐GOD (of CEL‐GOD) were Km = 0.15 ± 0.02 (0.43 ± 0.09) mmol L−1, Vmax = 0.18 ± 0.01 (0.21 ± 0.07) μmol L−1 s−1, and kcat/Km = 24.12 ± 0.52 (17.74 ± 0.85) s−1 mmol−1 L. Nearly 65% of the initial activity of GO‐CEL‐E/N‐GA‐GOD could be retained after seven cycles. Notably the conversion of gluconic acid was able to reach 63.82 ± 8.03% within 2 h. CONCLUSION Step‐by‐step immobilization method made full use of different functional groups on GO, avoiding the competition for fixed sites between CEL and GOD in the immobilization processes. The results reflected the feasibility of the strategy to build bio‐microsystem as CEL and GOD immobilized on GO by covalent bonds to achieve the conversion from CMC to gluconic acid in one‐step. © 2019 Society of Chemical Industry
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