Loss of photosynthesis signals a metabolic reprogramming to sustain sugar homeostasis during senescence of green leaves: Role of cell wall hydrolases

2018 ◽  
Vol 56 (1) ◽  
pp. 404-410 ◽  
Author(s):  
B. Biswal ◽  
J. K. Pandey
2019 ◽  
Author(s):  
◽  
Wanda Melissa Figueroa-Cuilan

The plant pathogen Agrobacterium tumefaciens displays an atypical form of unipolar elongation, followed by incipient pole synthesis during cell division and cell separation. Currently, how polar growing bacteria modulate cell wall hydrolysis during growth and division remains largely unknown. This work includes the comprehensive analysis and characterization of the role of cell wall hydrolyses involved in bacterial growth, division, recycling and beta-lactam resistance in A. tumefaciens. First, we performed bioinformatic analyses and used reverse genetics to better understand the role cell wall hydrolases in A. tumefaciens. Inactivation of most cell wall hydrolases, led to no phenotypic defects suggesting a high degree of redundancy. However, inactivation of the amidase, AmiD, and the lytic transglycosylase Atu3779, revealed significant changes in beta-lactam resistance suggesting that these proteins are involved in the activation beta-lactamases and outer-membrane integrity. Next, we developed a tool (Figueroa-Cuilan et al., 2016) to dissect the role of essential genes, which enabled characterization of the essential regulator of cell division, DipM, a LytM-containing factor. Absence of DipM causes severe cell division defects, including increased cell length, mid-cell width and lysis. A cell wall composition analysis of cells devoid of DipM shows an increase in the activity of the PG hydrolases, lytic transglycosylases, suggesting that DipM may inhibit the activity of these enzymes. Lastly, we find that deletion of individual lytic transglycolsylases (LTs) from the DipM depletion strain delays the onset of the DipM depletion phenotype. Overall, this research provides mechanistic insights about the roles of peptidoglycan hydrolases and their regulators in cell growth and division. Understanding how bacterial cell wall hydrolysis is spatiotemporally regulated and coordinated with cell wall synthesis and cell division (Figueroa-Cuilan and Brown, 2018), will be applicable to other closely related polar-growing bacteria.


2014 ◽  
Vol 106 (2) ◽  
pp. 579a
Author(s):  
Xiaoxue Zhou ◽  
David K. Halladin ◽  
Enrique R. Rojas ◽  
Julie A. Theriot

2002 ◽  
Vol 22 (1-2) ◽  
pp. 209-222 ◽  
Author(s):  
Bénédicte Flambard

2020 ◽  
Author(s):  
Ranjeet Singh Mahla ◽  
Akhilesh Kumar ◽  
Helena Tutil ◽  
Sreevidhya Tarakkad Krishnaji ◽  
Bharathwaj Sathyamoorthy ◽  
...  

2020 ◽  
Vol 2 (1) ◽  
Author(s):  
Fangwei Yu ◽  
Shenyun Wang ◽  
Wei Zhang ◽  
Hong Wang ◽  
Li Yu ◽  
...  

Abstract The members of myeloblastosis transcription factor (MYB TF) family are involved in the regulation of biotic and abiotic stresses in plants. However, the role of MYB TF in phosphorus remobilization remains largely unexplored. In the present study, we show that an R2R3 type MYB transcription factor, MYB103, is involved in phosphorus (P) remobilization. MYB103 was remarkably induced by P deficiency in cabbage (Brassica oleracea var. capitata L.). As cabbage lacks the proper mutant for elucidating the mechanism of MYB103 in P deficiency, another member of the crucifer family, Arabidopsis thaliana was chosen for further study. The transcript of its homologue AtMYB103 was also elevated in response to P deficiency in A. thaliana, while disruption of AtMYB103 (myb103) exhibited increased sensitivity to P deficiency, accompanied with decreased tissue biomass and soluble P concentration. Furthermore, AtMYB103 was involved in the P reutilization from cell wall, as less P was released from the cell wall in myb103 than in wildtype, coinciding with the reduction of ethylene production. Taken together, our results uncover an important role of MYB103 in the P remobilization, presumably through ethylene signaling.


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