My watch list  


Fructokinase (/fruc•to•ki•nase/ [-ki´nas]), also known as D-fructokinase or D-fructose (D-mannose) kinase,[1] is an enzyme of the liver, intestine, and kidney cortex. Fructokinase, with a length of approximately 2.6 angstroms, is in a family of enzymes called transferases, meaning that this enzyme transfers phosphorus containing groups; it is also considered a phosphotransferase, since it uses an alcohol group as an acceptor.[1] Fructokinase specifically catalyzes the transfer of a phosphate group from ATP (the substrate) to fructose as the initial step in its utilization.[1] The main role of fructokinase is in carbohydrate metabolism, more specifically, sucrose and starch metabolism. The reaction equation is as follows: ATP + D-fructose = ADP + D-fructose 6-phosphate.


Role in Plants and Bacteria

Fructokinase has been characterized from various organisms such as pea (Pisum sativum) seeds, avocado (Persera americana) fruit, and maize (Zea mays) kernels, and many more.[2]

Specifically, fructokinase may also regulate starch synthesis in conjunction with SS, sucrose synthase, which first metabolizes sink tissue in plant tissues such as in potatoes.[2] There are also two divergent fructokinase genes that are differentially expressed and which also have different enzymatic properties such as those found in tomatoes. In tomatoes, fructokinase 1 (Frk 1) mRNA is expressed at a constant level during fruit development. However, fructokinase 2 (Frk 2) mRNA has a high expression level in young tomato fruit but then decreases during the later stages of fruit development. Frk 2 has a higher affinity for fructose than Frk 1 but Frk 2 activity is inhibited by high levels of fructose, whereas Frk 1 activity is not.[2]

Role in Animals and Humans

In human liver, purified fructokinase, when coupled with aldolase, has been discovered to contribute to an alternative mechanism to produce oxalate from xylitol. In coupled sequence, fructokinase and aldolase produce glycolaldehyde, a precursor to oxalate, from D-xylulose via D-xylulose 1-phosphate.[3]

In rat liver cells (hepatocytes), GTP is also a substrate of fructokinase. It can be used at a substantial rate by fructokinase. In these isolated hepatocytes, in vivo, when the concentration of ATP falls to about 1 millimole in a short time interval, GTP becomes an important substrate under these specific conditions.[4]

ATP + D-Fructose = ADP + D-Fructose 6-phosphate[5]


Fructosuria or hepatic fructokinase deficiency is a rare but benign inherited metabolic disorder.[6] This condition is caused by a deficiency of fructokinase in the liver. Affected individuals usually display a large blood fructose concentration after the ingestion of fructose, sucrose or sorbitol.[7] The disease is mainly characterized by the detection of the abnormal excretion of fructose in the urine through a urinalysis. Fructokinase is needed for the synthesis of glycogen, the body's form of stored energy, from fructose. The presence of fructose in the blood and urine may lead to an incorrect diagnosis of diabetes mellitus. Symptoms that may lead to the eventual diagnosis of fructosuria are hepatic fructokinase deficiency, levulosuria and ketohexokinase deficiency.


  1. ^ a b c DBGET ENZYME: Retrieved 2007-05-06
  2. ^ a b c Odanaka S, Bennett AB, Kanayama Y (Jul 2002). "Distinct physiological roles of fructokinase isozymes revealed by gene-specific suppression of Frk1 and Frk2 expression in tomato". Plant Physiol. 129 (3): 1119-26. PMID 12114566.
  3. ^ James HM, Bais R, Edwards JB, Rofe AM, Conyers AJ (Feb 1982). "Models for the metabolic production of oxalate from xylitol in humans: a role for fructokinase and aldolase". The Australian journal of experimental biology and medical science 60 (Pt 1): 117-22. PMID 6284103.
  4. ^ Phillips MI, Davies DR (1985 Jun 15). "The mechanism of guanosine triphosphate depletion in the liver after a fructose load. The role of fructokinase". Biochem. J. 228 (3): 667-71. PMID 2992452.
  5. ^ BRENDA
  6. ^ WebMD Children's Health - Fructosuria. Retrieved 2007-05-06
  7. ^ Asipu A, Hayward BE, O'Reilly J, Bonthron DT (Sept 2003). "Properties of normal and mutant recombinant human ketohexokinases and implications for the pathogenesis of essential fructosuria". Diabetes 52 (9): 2426-32. PMID 12941785.
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Fructokinase". A list of authors is available in Wikipedia.
Your browser is not current. Microsoft Internet Explorer 6.0 does not support some functions on Chemie.DE