A thermostable mannitol‐1‐phosphate dehydrogenase is required in mannitol metabolism of the thermophilic acetogenic bacteriumThermoanaerobacter kivui

2019 ◽  
Vol 21 (10) ◽  
pp. 3728-3736 ◽  
Author(s):  
Jimyung Moon ◽  
Laura Henke ◽  
Nadine Merz ◽  
Mirko Basen
Keyword(s):  
2007 ◽  
Vol 44 (4) ◽  
pp. 258-268 ◽  
Author(s):  
Heriberto Vélëz ◽  
Norman J. Glassbrook ◽  
Margaret E. Daub

2013 ◽  
Vol 65 (2) ◽  
pp. 559-570 ◽  
Author(s):  
Agnès Groisillier ◽  
Zhanru Shao ◽  
Gurvan Michel ◽  
Sophie Goulitquer ◽  
Patricia Bonin ◽  
...  

BMC Genomics ◽  
2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Zhanru Shao ◽  
Pengyan Zhang ◽  
Chang Lu ◽  
Shaoxuan Li ◽  
Zhihang Chen ◽  
...  

Abstract Background Alginate is an important cell wall component and mannitol is a soluble storage carbon substance in the brown seaweed Saccharina japonica. Their contents vary with kelp developmental periods and harvesting time. Alginate and mannitol regulatory networks and molecular mechanisms are largely unknown. Results With WGCNA and trend analysis of 20,940 known genes and 4264 new genes produced from transcriptome sequencing of 30 kelp samples from different stages and tissues, we deduced that ribosomal proteins, light harvesting complex proteins and “imm upregulated 3” gene family are closely associated with the meristematic growth and kelp maturity. Moreover, 134 and 6 genes directly involved in the alginate and mannitol metabolism were identified, respectively. Mannose-6-phosphate isomerase (MPI2), phosphomannomutase (PMM1), GDP-mannose 6-dehydrogenase (GMD3) and mannuronate C5-epimerase (MC5E70 and MC5E122) are closely related with the high content of alginate in the distal blade. Mannitol accumulation in the basal blade might be ascribed to high expression of mannitol-1-phosphate dehydrogenase (M1PDH1) and mannitol-1-phosphatase (M1Pase) (in biosynthesis direction) and low expression of mannitol-2-dehydrogenase (M2DH) and Fructokinase (FK) (in degradation direction). Oxidative phosphorylation and photosynthesis provide ATP and NADH for mannitol metabolism whereas glycosylated cycle and tricarboxylic acid (TCA) cycle produce GTP for alginate biosynthesis. RNA/protein synthesis and transportation might affect alginate complex polymerization and secretion processes. Cryptochrome (CRY-DASH), xanthophyll cycle, photosynthesis and carbon fixation influence the production of intermediate metabolite of fructose-6-phosphate, contributing to high content of mannitol in the basal blade. Conclusions The network of co-responsive DNA synthesis, repair and proteolysis are presumed to be involved in alginate polymerization and secretion, while upstream light-responsive reactions are important for mannitol accumulation in meristem of kelp. Our transcriptome analysis provides new insights into the transcriptional regulatory networks underlying the biosynthesis of alginate and mannitol during S. japonica developments.


1992 ◽  
Vol 22 (8) ◽  
pp. 1157-1163 ◽  
Author(s):  
Wojtek P. Michalski ◽  
John A. Edgar ◽  
Stephen J. Prowse

2013 ◽  
Vol 4 ◽  
Author(s):  
Benoit Calmes ◽  
Thomas Guillemette ◽  
Lény Teyssier ◽  
Benjamin Siegler ◽  
Sandrine Pigné ◽  
...  

1970 ◽  
Vol 16 (5) ◽  
pp. 363-367 ◽  
Author(s):  
Wei Hwa Lee

Aspergillus species (UC4177) accumulated mannitol from glucose substrate and it also used mannitol as the sole carbon source. Experiment with radioactive mannitol showed that the accumulation of mannitol and the oxidation of mannitol to CO2 proceeded simultaneously. The presence of glucose in the medium did not inhibit mannitol oxidation. Mannitol was oxidized at about 25% of the metabolic rate of glucose. The rate of mannitol oxidation and several of the enzymes directly involved in mannitol metabolism were unaffected by using glucose or mannitol as the sole source of carbon. Nine enzymes of glucose metabolism were tested and none appeared to limit the rate of glucose oxidation. Aspergillus phosphofructokinase was not inhibited by 2.4 mM ATP or 10 mM citrate. Possible enzymatic defects favoring mannitol accumulation were not found.


2005 ◽  
Vol 7 (5) ◽  
pp. 407-415 ◽  
Author(s):  
Koji Iwamoto ◽  
Yoshihiro Shiraiwa
Keyword(s):  

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