Heterologous gene expression and characterization of recombinant aspartate aminotransferase from Geobacillus thermopakistaniensis

2020 ◽  
Vol 175 ◽  
pp. 105709
Author(s):  
Ghazaleh Gharib ◽  
Shahid Mahmood Chohan ◽  
Naeem Rashid ◽  
Muhammad Akhtar
2011 ◽  
Vol 30 (10) ◽  
pp. 751-761 ◽  
Author(s):  
Megan M. Multhaup ◽  
Sweta Gurram ◽  
Kelly M. Podetz-Pedersen ◽  
Andrea D. Karlen ◽  
Debra L. Swanson ◽  
...  

Extremophiles ◽  
2021 ◽  
Author(s):  
Ilma Fauziah Ma’ruf ◽  
Yuka Sasaki ◽  
Anastasia Kerbs ◽  
Jochen Nießer ◽  
Yu Sato ◽  
...  

Yeast ◽  
2009 ◽  
Vol 26 (10) ◽  
pp. 545-551 ◽  
Author(s):  
Dongmei Bai Flagfeldt ◽  
Verena Siewers ◽  
Le Huang ◽  
Jens Nielsen

1994 ◽  
Vol 25 (6) ◽  
pp. 524-530 ◽  
Author(s):  
Naoki Takaya ◽  
Koji Yanai ◽  
Hiroyuki Horiuchi ◽  
Akinori Ohta ◽  
Masamichi Takagi

2004 ◽  
Vol 186 (18) ◽  
pp. 6070-6076 ◽  
Author(s):  
Naeem Rashid ◽  
Tamotsu Kanai ◽  
Haruyuki Atomi ◽  
Tadayuki Imanaka

ABSTRACT Four orthologous genes (TK1108, TK1404, TK1777, and TK2185) that can be annotated as phosphomannomutase (PMM) genes (COG1109) have been identified in the genome of the hyperthermophilic archaeon Thermococcus kodakaraensis KOD1. We previously found that TK1777 actually encodes a phosphopentomutase. In order to determine which of the remaining three orthologues encodes a phosphoglucomutase (PGM), we examined the PGM activity in T. kodakaraensis cells and identified the gene responsible for this activity. Heterologous gene expression and purification and characterization of the recombinant protein indicated that TK1108 encoded a protein with high levels of PGM activity (690 U mg−1), along with high levels of PMM activity (401 U mg−1). Similar analyses of the remaining two orthologues revealed that their protein products exhibited neither PGM nor PMM activity. PGM activity and transcription of TK1108 in T. kodakaraensis were found to be higher in cells grown on starch than in cells grown on pyruvate. Our results clearly indicate that, among the four PMM gene orthologues in T. kodakaraensis, only one gene, TK1108, actually encodes a protein with PGM and PMM activities.


BioTechniques ◽  
2001 ◽  
Vol 30 (3) ◽  
pp. 474-476 ◽  
Author(s):  
Ichiro Matsumura ◽  
Mark J. Olsen ◽  
Andrew D. Ellington

Plants ◽  
2021 ◽  
Vol 10 (3) ◽  
pp. 524
Author(s):  
Bingqi Wu ◽  
Zhiting Chen ◽  
Xiaohui Xu ◽  
Ronghua Chen ◽  
Siwei Wang ◽  
...  

Functional characterization of plant agrichemical transporters provided an opportunity to discover molecules that have a high mobility in plants and have the potential to increase the amount of pesticides reaching damage sites. Agrobacterium-mediated transient expression in tobacco is simple and fast, and its protein expression efficiency is high; this system is generally used to mediate heterologous gene expression. In this article, transient expression of tobacco nicotine uptake permease (NtNUP1) and rice polyamine uptake transporter 1 (OsPUT1) in Nicotiana benthamiana was performed to investigate whether this system is useful as a platform for studying the interactions between plant transporters and pesticides. The results showed that NtNUP1 increases nicotine uptake in N. benthamiana foliar discs and protoplasts, indicating that this transient gene expression system is feasible for studying gene function. Moreover, yeast expression of OsPUT1 apparently increases methomyl uptake. Overall, this method of constructing a transient gene expression system is useful for improving the efficiency of analyzing the functions of plant heterologous transporter-encoding genes and revealed that this system can be further used to study the functions of transporters and pesticides, especially their interactions.


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