F0877
D-Fructose 1-phosphate barium salt
≥97%, crystalline
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About This Item
Fórmula lineal:
C6H11O9PBa
Número de CAS:
Peso molecular:
395.45
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
assay
≥97%
form
crystalline
storage temp.
−20°C
SMILES string
[Ba].OCC(O)C(O)C(O)C(=O)COP(O)(O)=O
Application
D-Fructose 1-phosphate is an effector of the metabolic regulator Cra of Pseudomonas putida and inhibitor of translation of SugR, a pleiotropic transcriptional repressor, in Corynebacterium glutamicum.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk_germany
WGK 1
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Haruhiko Teramoto et al.
Journal of biotechnology, 154(2-3), 114-125 (2011-02-01)
Corynebacterium glutamicum, a high-GC Gram-positive soil bacterium, has been used in development of bioprocesses for production of various compounds such as amino acids, organic acids, and alcohols. Recently, several transcriptional regulators, each of which is involved in multiple carbon metabolic
Fructose 1-phosphate is the preferred effector of the metabolic regulator Cra of Pseudomonas putida.
Max Chavarría et al.
The Journal of biological chemistry, 286(11), 9351-9359 (2011-01-18)
The catabolite repressor/activator (Cra) protein is a global sensor and regulator of carbon fluxes through the central metabolic pathways of gram-negative bacteria. To examine the nature of the effector (or effectors) that signal such fluxes to the protein of Pseudomonas
T M Ramseier
Research in microbiology, 147(6-7), 489-493 (1996-07-01)
The catabolite repressor-activator (Cra) protein controls the direction of carbon flux through metabolic pathways in enteric bacteria. Cra binds to the control regions of target genes and exerts a negative effect on the expression of genes encoding glycolytic and Entner-Doudoroff
Christiane Dietrich et al.
Microbiology (Reading, England), 155(Pt 4), 1360-1375 (2009-04-01)
Corynebacterium glutamicum is a biotin-auxotrophic bacterium and some strains efficiently produce glutamic acid under biotin-limiting conditions. In an effort to understand C. glutamicum metabolism under biotin limitation, growth of the type strain ATCC 13032 was investigated in batch cultures and
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