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合金型三金属纳米复合材料作为一种高效且可回收的固定化脂肪酶的固体基质。

Alloyed Trimetallic Nanocomposite as an Efficient and Recyclable Solid Matrix for Lipase Immobilization.

机构信息

School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013, China.

School of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu 212013, China.

出版信息

Langmuir. 2024 Apr 30;40(17):8921-8938. doi: 10.1021/acs.langmuir.4c00090. Epub 2024 Apr 16.

Abstract

In this work, a trimetallic (Ni/Co/Zn) organic framework (tMOF), synthesized by a solvothermal method, was calcinated at 400 and 600 °C and the final products were used as a support for lipase immobilization. The material annealed at 400 °C (Ni-Co-Zn@400) had an improved surface area (66.01 m/g) and pore volume (0.194 cm/g), which showed the highest enzyme loading capacity (301 mg/g) with a specific activity of 0.196 U/mg, and could protect the enzyme against thermal denaturation at 65 °C. The optimal pH and temperature for the lipase were 8.0 and 45 °C but could tolerate pH levels 7.0-8.0 and temperatures 40-60 °C. Moreover, the immobilized enzyme (Ni-Co-Zn@Lipase, Ni-Co-Zn@400@Lipase, or Ni-Co-Zn@600@Lipase) could be recovered and reused for over seven cycles maintaining 80, 90, and 11% of its original activity and maintained a residual activity >90% after 40 storage days. The remarkable thermostability and storage stability of the immobilized lipase suggest that the rigid structure of the support acted as a protective shield against denaturation, while the improved pH tolerance toward the alkaline range indicates a shift in the ionization state attributed to unequal partitioning of hydroxyl and hydrogen ions within the microenvironment of the active site, suggesting that acidic residues may have been involved in forming an enzyme-support bond. The high enzyme loading capacity, specific activity, encouraging stability, and high recoverability of the tMOF@Lipase indicate that a multimetallic MOF could be a better platform for efficient enzyme immobilization.

摘要

在这项工作中,通过溶剂热法合成了一种三金属(Ni/Co/Zn)有机框架(tMOF),并在 400 和 600°C 下煅烧,最终产物用作脂肪酶固定化的载体。在 400°C 下退火的材料(Ni-Co-Zn@400)具有改善的表面积(66.01 m/g)和孔体积(0.194 cm/g),显示出最高的酶负载能力(301 mg/g),比活为 0.196 U/mg,并且能够在 65°C 下保护酶免受热变性。脂肪酶的最佳 pH 和温度分别为 8.0 和 45°C,但可以耐受 pH 值 7.0-8.0 和温度 40-60°C。此外,固定化酶(Ni-Co-Zn@Lipase、Ni-Co-Zn@400@Lipase 或 Ni-Co-Zn@600@Lipase)可以回收并重复使用超过七次,保持其原始活性的 80%、90%和 11%,并且在 40 天的储存后保持 90%以上的剩余活性。固定化脂肪酶的显著热稳定性和储存稳定性表明载体的刚性结构起到了防止变性的保护作用,而对碱性范围的 pH 耐受性提高表明了电离状态的转变归因于微环境中羟基和氢离子的分配不均等,这表明酸性残基可能参与了形成酶-载体键。tMOF@Lipase 的高酶负载能力、比活、令人鼓舞的稳定性和高回收率表明,多金属 MOF 可能是高效酶固定化的更好平台。

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