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利用冰核蛋白实现细菌表面展示磷酸盐结合蛋白提高磷酸盐的吸附。

Improved phosphate biosorption by bacterial surface display of phosphate-binding protein utilizing ice nucleation protein.

机构信息

State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.

出版信息

FEMS Microbiol Lett. 2009 Oct;299(1):44-52. doi: 10.1111/j.1574-6968.2009.01724.x. Epub 2009 Jul 13.

Abstract

The conventional enhanced biological phosphorus removal (EBPR) system often deteriorates at low chemical oxygen demand (COD) or under aeration conditions. A new approach that incorporates phosphate-eutrophic wastewater remediation was introduced through immobilization of an intracellular phosphate-binding protein (PBP) onto the surface of Pseudomonas putida or Escherichia coli, using the N-terminal anchor (InaQ-N) of a newly identified ice nucleation protein from Pseudomonas syringae. A green fluorescent protein-fusion protein was expressed and used to confirm surface localization. The PBP was then targeted to the surface of E. coli JM109 and P. putida AB92019. The engineered P. putida and E. coli microorganisms were capable of absolute biosorption of total phosphates at rates of 60 and 80 mg L(-1), respectively, over 5 h. In the recombinant P. putida cells, a surface-immobilized PBP fusion that had three tandemly repeated InaQ-Ns exhibited the maximum increment in phosphate biosorption, at sixfold compared with the control strain. Even heat-killed recombinant cells of either P. putida or E. coli retained substantial biosorptive activities. The current study demonstrates that the bacterial surface display of PBP should be considered as a strong contender for generating organisms capable of functioning in EBPR systems under low COD, resulting in improved removal of eutrophic phosphorus from wastewaters.

摘要

传统的强化生物除磷(EBPR)系统在低化学需氧量(COD)或曝气条件下往往会恶化。一种新的方法是通过将细胞内磷酸盐结合蛋白(PBP)固定在假单胞菌或大肠杆菌的表面,利用从丁香假单胞菌中新鉴定的冰核蛋白的 N 端锚(InaQ-N)来引入磷酸盐富营养废水修复。表达了绿色荧光蛋白融合蛋白,并用于确认表面定位。然后将 PBP 靶向大肠杆菌 JM109 和 Pseudomonas putida AB92019。工程化的 Pseudomonas putida 和 Escherichia coli 微生物能够在 5 小时内分别以 60 和 80 mg L(-1)的速率绝对吸附总磷酸盐。在重组 Pseudomonas putida 细胞中,表面固定的 PBP 融合体具有三个串联的 InaQ-N,与对照菌株相比,磷酸盐生物吸附的最大增量增加了六倍。即使是热灭活的 Pseudomonas putida 或 Escherichia coli 的重组细胞仍保留了相当大的生物吸附活性。本研究表明,应考虑将 PBP 的细菌表面展示作为产生能够在低 COD 下在 EBPR 系统中运行的生物体的有力竞争者,从而从废水中更好地去除富营养磷。

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