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Updated: Feb 11, 2026

Protein Engineering by Yeast Surface Display
Published on: November 29, 2024
Engineering immobilized microbes with surface-displayed cold-adapted nitroreductase: An efficient strategy for
Yanhua Hou1, Yujie Li1, Yifan Zou1
1School of Marine Science and Technology, Harbin Institute of Technology, Weihai, 264209, China.
None:
Nitrobenzene (NB), a typical example of aromatic nitro compounds, has become a significant pollutant because its wastewater is difficult to degrade in low-temperature environments. This study constructed an engineered strain displaying a cold-adapted nitroreductase (PsNTR) for enhanced low-temperature degradation efficiency, employing a cell surface display system in which the N-terminal domain of the ice nucleation protein (INPN) served as the anchoring carrier. SDS-PAGE, Western blot analysis, and protease accessibility assays confirmed that the INPN-PsNTR fusion protein (55.40 kDa) was stably expressed and displayed on the surface of Escherichia coli. The engineered strain BL21/INPN-PsNTR maintained outer membrane integrity and exhibited robust growth during the display process. To further enhance the storage stability and reusability of the engineered strain for practical applications, it was immobilized using modified diatomite (DA-PEI/GA). Notably, PsNTR@DA-PEI/GA demonstrated high efficiency in degrading NB at low temperatures, with a degradation rate of 92.75% for 500 mg/L NB within 120 h at 15 °C. In summary, this study employed PsNTR surface display technology as the core strategy, combined with a cell immobilization approach, to establish a novel and promising technological pathway for efficient and green degradation of NB at low temperatures, thereby offering a new strategy for the remediation of NB contamination.
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