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D-ribulose 1-phosphate is a key intermediate in the Calvin cycle, a series of biochemical reactions that occur in plants, algae, and some bacteria, facilitating the fixation of carbon dioxide into organic molecules. This five-carbon sugar phosphate compound plays a crucial role in the process of photosynthesis, where it is involved in the conversion of carbon dioxide into glucose. D-ribulose 1-phosphate is formed from the condensation of two molecules of xylulose 5-phosphate, catalyzed by the enzyme ribulose-phosphate carboxylase/oxygenase (RuBisCO). It is then isomerized to form 3-phosphoglycerate, which is subsequently reduced to glyceraldehyde 3-phosphate, a precursor for glucose synthesis. The compound's involvement in the Calvin cycle highlights its importance in the global carbon cycle and the production of energy-rich compounds necessary for life on Earth.

7721-50-8

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7721-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7721-50-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,2 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7721-50:
(6*7)+(5*7)+(4*2)+(3*1)+(2*5)+(1*0)=98
98 % 10 = 8
So 7721-50-8 is a valid CAS Registry Number.

7721-50-8Downstream Products

7721-50-8Relevant academic research and scientific papers

Facile Enzymatic Synthesis of Phosphorylated Ketopentoses

Wen, Liuqing,Huang, Kenneth,Liu, Yunpeng,Wang, Peng George

, p. 1649 - 1654 (2016)

An efficient and convenient platform for the facile synthesis of phosphorylated ketoses is described. All eight phosphorylated ketopentoses were produced using this platform starting from two common and inexpensive aldoses (d-xylose and l-arabinose) in more than 84% isolated yield (gram scale). In this method, reversible conversions (isomerization or epimerization) were accurately controlled toward the formation of desired ketose phosphates by targeted phosphorylation reactions catalyzed by substrate-specific kinases. The byproducts were selectively removed by silver nitrate precipitation avoiding the tedious and time-consuming separation of sugar phosphate from adenosine phosphates (ATP and ADP). Moreover, the described strategy can be expanded for the synthesis of other sugar phosphates.

Facile enzymatic synthesis of ketoses

Wen, Liuqing,Huang, Kenneth,Wei, Mohui,Meisner, Jeffrey,Liu, Yunpeng,Garner, Kristina,Zang, Lanlan,Wang, Xuan,Li, Xu,Fang, Junqiang,Zhang, Houcheng,Wang, Peng George

supporting information, p. 12654 - 12658 (2015/10/28)

Studies of rare ketoses have been hampered by a lack of efficient preparation methods. A convenient, efficient, and cost-effective platform for the facile synthesis of ketoses is described. This method enables the preparation of difficult-to-access ketopentoses and ketohexoses from common and inexpensive starting materials with high yield and purity and without the need for a tedious isomer separation step. A spoonful of sugar: A convenient, efficient, and cost-effective platform for the facile synthesis of ketoses is described. This method, which involves a one-pot mulitenzyme (OPME) reaction, enables the preparation of rare ketopentoses and ketohexoses from common and inexpensive starting materials with high yield and purity and without the need for a tedious isomer separation step.

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