A novel strategy for constructing N-terminal chromosomal fusions to green fluorescent protein in the yeastSaccharomyces cerevisiae

FEBS Letters ◽  
2000 ◽  
Vol 485 (1) ◽  
pp. 29-34 ◽  
Author(s):  
Birgit Prein ◽  
Klaus Natter ◽  
Sepp D Kohlwein
Sensors ◽  
2019 ◽  
Vol 19 (8) ◽  
pp. 1846 ◽  
Author(s):  
Woonwoo Lee ◽  
Hyojin Kim ◽  
Yerin Kang ◽  
Youngshim Lee ◽  
Youngdae Yoon

Microbial cell-based biosensors, which mostly rely on stress-responsive operons, have been widely developed to monitor environmental pollutants. Biosensors are usually more convenient and inexpensive than traditional instrumental analyses of environmental pollutants. However, the targets of biosensors are restricted by the limited number of genetic operon systems available. In this study, we demonstrated a novel strategy to overcome this limitation by engineering an enhanced green fluorescent protein (eGFP). It has been reported that combining two fragments of split-eGFP can form a native structure. Thus, we engineered new biosensors by inserting metal-binding loops (MBLs) between β-strands 9 and 10 of the eGFP, which then undergoes conformational changes upon interaction between the MBLs and targets, thereby emitting fluorescence. The two designed MLBs based on our previous study were employed as linkers between two fragments of eGFP. As a result, an Escherichia coli biosensor exhibited a fluorescent signal only when interacting with cadmium ions, revealing the prospect of a new biosensor for cadmium detection. Although this study is a starting stage for further developing biosensors, we believe that the proposed strategy can serve as basis to develop new biosensors to target various environmental pollutants.


2015 ◽  
Vol 86 (5) ◽  
pp. 1242-1252 ◽  
Author(s):  
Luyen T. Vu ◽  
Thanh T. K. Nguyen ◽  
Shafiul Alam ◽  
Takashi Sakamoto ◽  
Kenzo Fujimoto ◽  
...  

2014 ◽  
Vol 50 (67) ◽  
pp. 9547-9549 ◽  
Author(s):  
Dongmei Xi ◽  
Xindong Wang ◽  
Shiyun Ai ◽  
Shusheng Zhang

A novel strategy was developed for cancer cell detection using triplex DNA based on expression of enhanced green fluorescent protein.


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