journal article·2024-08-21

Effects of Cross-linker Chemistry on Bioelectrocatalytic Reactions in a Redox Cross-linked Network of Glucose Dehydrogenase and Thionine

Md Motaher Hossain, Muhammad Rezki, Ibrahim Shalayel, Abdelkader Zebda, Seiya Tsujimura

ACS Applied Materials & Interfaces· Volume 16· Issue 33
Publisher page

Abstract

Enzyme-mediator bioconjugation is emerging as a building block for designing electrode platforms for the construction of biosensors and biofuel cells. Here, we report a one-pot bioconjugation technique for flavin adenine dinucleotide-dependent glucose dehydrogenase (FAD-GDH) and thionine (TH) using a series of cross-linkers, including epoxy, N -hydroxysuccinimide (NHS), and aldehydes. In this technique, FAD-GDH and thionine are conjugated through an amine cross-linking reaction to generate a redox network, which has been successfully employed for the oxidation of glucose. The bioconjugation chemistry of cross-linkers with the amino groups on FAD-GDH and thionine plays a vital role in generating distinct network structures. The epoxy-type cross-linker reacts with the primary and secondary amines of thionine at room temperature, thereby producing an FAD-GDH-TH-FAD-GDH hyperbranched bioconjugate network, the aldehyde undergoes a rapid cross-linking reaction to produce a network of FAD-GDH-FAD-GDH, while the NHS-based cross-linker can react with the primary amines of both FAD-GDH and thionine, forming an FAD-GDH-cross-linker-TH polymeric network. This reaction has the potential to enable the conjugation of a redox mediator with a FAD-GDH network, which is particularly essential when designing an enzyme electrode platform. The data demonstrated that the polymeric cross-linked network based on the NHS cross-linker exhibited a considerable increase in electron transport while producing a catalytic current of 830 μA cm –2 . The cross-linker spacer arm length also affects the overall electrochemical function of the network and its performance; an adequate spacer length containing a cross-linker is required, resulting in a faster electron transfer. Finally, a leaching test confirmed that the stability of the enzyme electrode was improved when the electrode was tested using the redox probe. This study elucidates the relationship between cross-linking chemistry and redox network structure and enhances the high performance of enzyme electrode platforms for the oxidation of glucose.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrochemical sensors and biosensors · Electrochemical Analysis and Applications · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Materials Science, Institute of Pure and Applied Sciences, University of Tsukuba, 1-1-1, Tennodai, Tsukuba, Ibaraki 305-5358, Japan

TIMC-IMAG/CNRS/INSERM, UMR 5525, Université Grenoble Alpes, Grenoble 38000, France

Japanese-French Laboratory for Semiconductor Physics and Technology (J-FAST), CNRS-Université Grenoble Alpes, Grenoble 38000, France

Funding

Japan Science and Technology Agency

References (70)

Show source-provided references
1. 10.1080/09168451.2018.152720910.1080/09168451.2018.1527209 ↗
2. 10.1039/D0CS00304B10.1039/D0CS00304B ↗
3. 10.1039/c3cp44617d10.1039/c3cp44617d ↗
4. 10.1021/acs.langmuir.5b0474210.1021/acs.langmuir.5b04742 ↗
5. 10.1271/bbb.70.65410.1271/bbb.70.654 ↗
6. 10.1016/j.bios.2021.11335710.1016/j.bios.2021.113357 ↗
7. 10.1177/19322968110050050710.1177/193229681100500507 ↗
8. 10.1016/j.electacta.2014.05.08810.1016/j.electacta.2014.05.088 ↗
9. 10.1007/s00216-011-5650-710.1007/s00216-011-5650-7 ↗
10. 10.1021/ac202647z10.1021/ac202647z ↗
11. 10.1016/j.bios.2012.11.03610.1016/j.bios.2012.11.036 ↗
12. 10.1016/j.bioelechem.2018.04.00710.1016/j.bioelechem.2018.04.007 ↗
13. 10.1016/j.elecom.2015.04.01310.1016/j.elecom.2015.04.013 ↗
14. 10.3390/ijms1803060410.3390/ijms18030604 ↗
15. 10.1039/C5SC01538C10.1039/C5SC01538C ↗
16. 10.1016/j.electacta.2016.06.07810.1016/j.electacta.2016.06.078 ↗
17. 10.1039/D1CC01707A10.1039/D1CC01707A ↗
18. 10.1039/C8TA10644D10.1039/C8TA10644D ↗
19. 10.1016/j.electacta.2013.02.08310.1016/j.electacta.2013.02.083 ↗
20. 10.1016/j.bios.2023.11527210.1016/j.bios.2023.115272 ↗
21. 10.1021/ar00173a00210.1021/ar00173a002 ↗
22. 10.1021/ac00202a00710.1021/ac00202a007 ↗
23. 10.1021/j100168a04610.1021/j100168a046 ↗
24. 10.1021/ac00071a03110.1021/ac00071a031 ↗
25. 10.1021/ja029510e10.1021/ja029510e ↗
26. 10.1021/j100144a01910.1021/j100144a019 ↗
27. 10.1021/ja00035a02510.1021/ja00035a025 ↗
28. 10.1016/0022-0728(95)04080-810.1016/0022-0728(95)04080-8 ↗
29. 10.1039/FT996920413110.1039/FT9969204131 ↗
30. 10.1021/ja016316410.1021/ja0163164 ↗
31. 10.1039/C3RA45991H10.1039/C3RA45991H ↗
32. 10.1149/2.026307jes10.1149/2.026307jes ↗
33. 10.1021/ac303579410.1021/ac3035794 ↗
34. 10.1016/j.jpowsour.2023.23399210.1016/j.jpowsour.2023.233992 ↗
35. 10.1007/s00289-013-0942-z10.1007/s00289-013-0942-z ↗
36. 10.1002/app.4738310.1002/app.47383 ↗
37. 10.1002/app.4887410.1002/app.48874 ↗
38. 10.1002/pola.2016910.1002/pola.20169 ↗
39. 10.1016/j.coelec.2019.03.00310.1016/j.coelec.2019.03.003 ↗
40. 10.1002/ange.20180339710.1002/ange.201803397 ↗
41. 10.1021/jacs.5b1195310.1021/jacs.5b11953 ↗
42. 10.1021/cr068069y10.1021/cr068069y ↗
43. 10.1016/j.eurpolymj.2019.10946010.1016/j.eurpolymj.2019.109460 ↗
44. 10.1039/c2tb00117a10.1039/c2tb00117a ↗
45. 10.1039/D2RA05151F10.1039/D2RA05151F ↗
46. 10.1021/acsomega.9b0188410.1021/acsomega.9b01884 ↗
47. 10.1021/acssuschemeng.5b0009510.1021/acssuschemeng.5b00095 ↗
48. 10.1021/acs.bioconjchem.3c0012710.1021/acs.bioconjchem.3c00127 ↗
49. 10.3390/ijms1803060410.3390/ijms18030604 ↗
50. 10.1016/j.bios.2011.03.01210.1016/j.bios.2011.03.012 ↗
51. 10.18494/SAM389410.18494/SAM3894 ↗
52. 10.1021/acs.biomac.0c0072210.1021/acs.biomac.0c00722 ↗
53. 10.1021/acs.nanolett.0c0303310.1021/acs.nanolett.0c03033 ↗
54. 10.1002/jctb.144110.1002/jctb.1441 ↗
55. 10.1021/acs.macromol.2c0059310.1021/acs.macromol.2c00593 ↗
56. 10.2144/04375RV0110.2144/04375RV01 ↗
57. 10.1021/jp071001h10.1021/jp071001h ↗
58. 10.1016/j.polymer.2016.07.03810.1016/j.polymer.2016.07.038 ↗
59. 10.1021/jacsau.2c0012010.1021/jacsau.2c00120 ↗
60. 10.1021/acs.macromol.1c0051310.1021/acs.macromol.1c00513 ↗
61. 10.1016/j.cbpa.2006.09.01810.1016/j.cbpa.2006.09.018 ↗
62. 10.1007/s00216-008-2231-510.1007/s00216-008-2231-5 ↗
63. 10.1016/0304-4173(85)90014-X10.1016/0304-4173(85)90014-X ↗
64. 10.1073/pnas.040802910210.1073/pnas.0408029102 ↗
65. 10.1021/acsaem.1c0060410.1021/acsaem.1c00604 ↗
66. 10.1016/j.talanta.2019.12021810.1016/j.talanta.2019.120218 ↗
67. 10.1021/acs.analchem.7b0286310.1021/acs.analchem.7b02863 ↗
68. 10.1016/0022-0728(86)90101-410.1016/0022-0728(86)90101-4 ↗
69. 10.1016/S0022-0728(80)80058-110.1016/S0022-0728(80)80058-1 ↗
70. 10.1021/acs.macromol.3c0041110.1021/acs.macromol.3c00411 ↗