- Alkaline phosphatase
Alkaline phosphatase (ALP) (EC number|3.1.3.1) is a
hydrolase enzyme responsible for removingphosphate groups from many types of molecules, includingnucleotides ,proteins , andalkaloids . The process of removing the phosphate group is called "dephosphorylation". As the name suggests, alkaline phosphatases are most effective in analkaline environment.Bacterial
In bacteria, alkaline phosphatase is located in the
periplasmic space , external to thecell membrane . Since this space is much more subject to environmental variation than the actual interior of the cell, bacterial alkaline phosphatase is comparatively resistant to inactivation, denaturation, anddegradation , and also has a higher rate of activity. Although the actual purpose of the enzyme is still not fully understood, the simple hypothesis, that it is a means for the bacteria to generate free phosphate groups for uptake and use, is supported by the fact that alkaline phosphatase is usually only produced by the bacteria during phosphate starvation and not when phosphate is plentiful. However, other possibilities exist; for instance, the presence of phosphate groups usually preventsorganic molecule s from passing through the membrane, therefore dephosphorylating them may be important for bacterial uptake of organic compounds in the wild. Some complexities of bacterialregulation andmetabolism suggest that other, more subtle, purposes for the enzyme may also play a role for the cell. In thelaboratory , however,mutant "Escherichia coli " lacking alkaline phosphatase survive quite well, as do mutants unable to shut off alkaline phosphatase production.Use in research
The most common alkaline phosphatases used in research are:
* Bacterial alkaline phosphatase (BAP), from "Escherichia coli " C4 cells
*Shrimp alkaline phosphatase (SAP) , from a species of Arcticshrimp ("Pandalus borealis ")
* Calf intestine alkaline phosphatase (CIAP), fromcalf intestine
*Placenta l alkaline phosphatase (PLAP) and its C terminally truncated version that lacks the last 24 amino acids (constituting the transmembrane domain) - the secreted alkaline phosphatase (SEAP)Alkaline phosphatase has become a useful tool in
molecular biology laboratories, sinceDNA normally possesses phosphate groups on the 5' end. Removing these phosphates prevents the DNA from ligating (the 5' end attaching to the 3' end), thereby keeping DNA molecules linear until the next step of the process for which they are being prepared; also, removal of the phosphate groups allowsradiolabeling (replacement by radioactive phosphate groups) in order to measure the presence of the labeled DNA through further steps in the process or experiment. For these purposes, the alkaline phosphatase from shrimp is the most useful, as it is the easiest to inactivate once it has done its job.Another important use of alkaline phosphatase is as a label for
enzyme immunoassay s.One common use in the dairy industry is as a marker of pasteurisation. This molecule is denatured by elevated temperatures found during pasteurisation, and can be tested for via colour change of a para-nitro-phenol phosphate substrate in a buffered solution (Aschaffenburg Mullen Test). Raw milk would typically produce a yellow colouration within a couple of minutes, whereas properly pasteurised milk should show no change. There are of course exceptions to this in the case of heat stable alkaline phophatases produced by some bacteria.
Inhibitors
All mammalian alkaline phosphatase isoenzymes except
placenta l (PLAP and SEAP) are inhibited byhomoarginine and similarly all except the intestinal and placental ones are blocked bylevamisole . Heating for ~2 hours at 65oC inactivated most isoenzymes except Placental isoforms (PLAP and SEAP).Human
protein
Name = alkaline phosphatase, intestinal
caption =
width =
HGNCid = 437
Symbol = ALPI
AltSymbols =
EntrezGene = 248
OMIM = 171740
RefSeq = NM_001631
UniProt = P09923
PDB =
ECnumber = 3.1.3.1
Chromosome = 2
Arm = q
Band = 37.1
LocusSupplementaryData = protein
Name = alkaline phosphatase, liver/bone/kidney
caption =
width =
HGNCid = 438
Symbol =ALPL
AltSymbols = HOPS
EntrezGene = 249
OMIM = 171760
RefSeq = NM_000478
UniProt = P05186
PDB =
ECnumber = 3.1.3.1
Chromosome = 1
Arm = p
Band = 36.12
LocusSupplementaryData = protein
Name = alkaline phosphatase, placental (Regan isozyme)
caption =
width =
HGNCid = 439
Symbol =ALPP
AltSymbols =
EntrezGene = 250
OMIM = 171800
RefSeq = NM_001632
UniProt = P05187
PDB =
ECnumber = 3.1.3.1
Chromosome = 2
Arm = q
Band = 37.1
LocusSupplementaryData =Physiology
In humans, alkaline phosphatase is present in all tissues throughout the entire body, but is particularly concentrated in
liver ,bile duct ,kidney ,bone , and theplacenta . The optimal pH for the enzyme activity is pH=10Fact|date=June 2007 in standard conditions (298K,1 atm).Diagnostic use
High ALP levels can show that the
bile duct s are blocked. [ [http://www.labtestsonline.org/understanding/analytes/alp/test.html ALP: The Test ] ] Levels are significantly higher in children and pregnant women.Lowered levels of ALP are less common than elevated levels.
The following conditions can cause abnormal levels of ALP:
Elevated levels (hyperphosphatasemia)
If it is unclear why alkaline phosphatase is elevated,
isoenzyme studies usingelectrophoresis can confirm the source of the ALP. Heat stability also distinguishes bone and liver isoenzymes ("bone burns, liver lasts").*
Liver (Liver ALP):
**Cholestasis ,cholecystitis ,cholangitis ,cirrhosis ,hepatitis ,fatty liver ,liver tumor , livermetastase s,drug intoxication
***N.B. concurrently elevated GGT(gamma glutamyl transpeptidase ) helps rule in favor of liver metastasis (rather than bone, kidney, etc.) when assessing spread of cancer.
** Drugs: e.g.verapamil ,carbamazepine ,phenytoin ,erythromycin ,allopurinol ,ranitidine
*Bone disease (Bone ALP):
**Paget's disease ,osteosarcoma , bone metastases ofprostatic cancer (High / very high ALP values)
** Other bonemetastases
** Fractured bone
**Multiple myeloma (only when associated with fractures)
*Skeletal involvement of other primary diseases:
**Osteomalacia ,rickets ,vitamin D deficiency , (Moderate rise)
** Malignanttumors (ALP originating from tumor)
**Renal disease (secondaryhyperparathyroidism )
** Primaryhypothyroidism
*Polycythemia vera
*Myelofibrosis
*Leukemoid reaction to infection
* Women usinghormonal contraception
*Pregnancy
*Biliary obstruction
* Transient hyperphosphatasaemia of infancy:benign , often associated with infectionLowered levels (hypophosphatasemia)
*
Hypophosphatasia , anautosomal recessive disease
* Postmenopausal women receivingestrogen therapy because ofosteoporosis
* Men with recentheart surgery ,malnutrition ,magnesium deficiency,hypothyroidism or severeanemia
* Children withachondroplasia andcretinism
* Children after a severeenteritis
*Pernicious anemia
*Aplastic anemia
*Chronic myelogenous leukemia Other notes
Leukocyte alkaline phosphatase (LAP) is found within
white blood cell s. Blood levels of LAP can help in the diagnosis ofchronic myelogenous leukemia (CML),polycythemia vera , and theleukemoid reaction .ee also
*
Liver function tests
*Acid phosphatase References
External links
* [http://www.chem.qmw.ac.uk/iubmb/enzyme/EC3/1/3/1.html IUBMB Enzyme Nomenclature]
* [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1525473&dopt=Abstract Structure and Mechanism of Alkaline Phosphatase]
* [http://www.turnerbiosystems.com/doc/appnotes/S_0096.php] [Veritas™ Microplate Luminometer Method for Alkaline Phosphatase
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