GltC, THE POSITIVE REGULATOR OF GLUTAMATE SYNTHASE GENE EXPRESSION

Author(s):  
D.E. Bohannon ◽  
A.L. Sonenshein
2021 ◽  
Vol 22 (14) ◽  
pp. 7328
Author(s):  
Yang Chen ◽  
Mi Zhang ◽  
Lei Wang ◽  
Xiaohan Yu ◽  
Xianbi Li ◽  
...  

Verticillium wilt, caused by Verticillium dahliae, is a devastating disease for many important crops, including cotton. Kiwellins (KWLs), a group of cysteine-rich proteins synthesized in many plants, have been shown to be involved in response to various phytopathogens. To evaluate genes for their function in resistance to Verticillium wilt, we investigated KWL homologs in cotton. Thirty-five KWL genes (GhKWLs) were identified from the genome of upland cotton (Gossypium hirsutum). Among them, GhKWL1 was shown to be localized in nucleus and cytosol, and its gene expression is induced by the infection of V. dahliae. We revealed that GhKWL1 was a positive regulator of GhERF105. Silencing of GhKWL1 resulted in a decrease, whereas overexpression led to an increase in resistance of transgenic plants to Verticillium wilt. Interestingly, through binding to GhKWL1, the pathogenic effector protein VdISC1 produced by V. dahliae could impair the defense response mediated by GhKWL1. Therefore, our study suggests there is a GhKWL1-mediated defense response in cotton, which can be hijacked by V. dahliae through the interaction of VdISC1 with GhKWL1.


Forests ◽  
2020 ◽  
Vol 11 (12) ◽  
pp. 1336
Author(s):  
Guizhi Fan ◽  
Tingting Zhang ◽  
Yingtian Liu ◽  
Yaguang Zhan ◽  
Baojiang Zheng

Putrescine (Put) can enhance secondary metabolite production, but its intrinsic regulatory mechanism remains unclear. In this study, Put treatment promoted betulin production and gene expression of lupeol synthase (LUS), one of betulin synthetic enzymes. The maximum betulin content and gene expression level of LUS was 4.25 mg·g−1 DW and 8.25 at 12 h after 1 mmol·L−1 Put treatment, approximately two- and four-times that in the control, respectively. Put treatment increased the content of nitric oxide (NO) and its biosynthetic enzyme activity of nitrate reductase (NR) and NO synthase (NOS). Pretreatment of the birch suspension cells with NO-specific scavenger 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline- 1-oxyl-3-oxide (cPTIO), NR inhibitor sodium azide (NaN3), and NOS inhibitor NG-nitro-L-Arg methyl ester (L-NAME) decreased Put-triggered NO generation and blocked Put-induced betulin production. Put treatment improved the content of NH4+ and its assimilation enzyme activity of glutamate synthase and glutamate dehydrogenase. NH4+ supplementation also promoted NO and betulin production. Thus, the above data indicated that Put-induced NO was essential for betulin production. NO derived from NR, NOS, and NH4+ mediated betulin production in birch suspension cell cultures under Put treatment.


1994 ◽  
Vol 161 (5) ◽  
pp. 404-408
Author(s):  
J. Michiels ◽  
I. D'hooghe ◽  
C. Verreth ◽  
H. Pelemans ◽  
J. Vanderleyden

1994 ◽  
Vol 161 (5) ◽  
pp. 404-408 ◽  
Author(s):  
Jan Michiels ◽  
Inge D'hooghe ◽  
Christel Verreth ◽  
Heidi Pelemans ◽  
Jos Vanderleyden

2000 ◽  
Vol 182 (21) ◽  
pp. 5939-5947 ◽  
Author(s):  
Boris R. Belitsky ◽  
Lewis V. Wray ◽  
Susan H. Fisher ◽  
Dian E. Bohannon ◽  
Abraham L. Sonenshein

ABSTRACT Synthesis of glutamate, the cell's major donor of nitrogen groups and principal anion, occupies a significant fraction of bacterial metabolism. In Bacillus subtilis, the gltABoperon, encoding glutamate synthase, requires a specific positive regulator, GltC, for its expression. In addition, the gltABoperon was shown to be repressed by TnrA, a regulator of several other genes of nitrogen metabolism and active under conditions of ammonium (nitrogen) limitation. TnrA was found to bind directly to a site immediately downstream of the gltAB promoter. As is true for other genes, the activity of TnrA at the gltAB promoter was antagonized by glutamine synthetase under certain growth conditions.


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