د "گلايکوليسېز" د بڼو تر مېنځ توپير

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و robot Adding: ro:Glicoliza
Xqbot (خبرې اترې | ونډې)
و robot Modifying: ro:Glicoliză; cosmetic changes
۱ کرښه:
{{ژباړل}}
:''دا هم وګورۍ: [[ګلوکونيوجنېسېز]], which carries out a process wherein glucose is synthesized rather than catabolized.''
'''ګلايکوليسېز''' د ګڼ شمېر تعاملونو د لړۍ نوم دی چې ګلوکوز په پايروېټ بدلوي او ورسره يو مقدار اډينوسين ټرايفاسفېټ هم توليدوي.دا تړنګنوم د [[يوناني ژبه|يوناني]] ژبې د وييکو ''γλυκύς'' (خوږ) او ''λύσις'' (حل کېدنه) څخه جوړ شوی.
 
ګلايکوليسېز يوه مېټابوليکي پروسه ده چې په دې پروسه کې ګلوکوز يا قنديات په پايروېټ بدلېږي. د همدې پروسې د ترسره کېدو وروسته چې کومه انرژي په لاس راځي هغه د هغې لوړې انرژۍ لرونکي مرکبونو په جوړېدنه کې لکه، د ATP اډېنوسين ټرای فاسفېټ او NADH نيکوټين اډېنين ډای نيوکليوټايډ کارېږي.
۷ کرښه:
 
It is the initial process of most [[carbohydrate catabolism]], and it serves three principal functions:
# Generation of high-energy molecules ([[Adenosine triphosphate|ATP]] and [[NADH]]) as cellular energy sources as part of [[aerobic respiration]] and [[anaerobic respiration]]; that is, in the former process, oxygen is present, and, in the latter, oxygen is not present
# Production of pyruvate for the [[citric acid cycle]] as part of [[aerobic respiration]]
# Production of a variety of six- and three-carbon intermediate compounds, which may be removed at various steps in the process for other cellular purposes.
 
As the foundation of both [[aerobic respiration|aerobic]] and [[anaerobic respiration]], glycolysis is the archetype of universal [[metabolism|metabolic]] processes known and occurring (with variations) in many types of [[Cell (biology)|cells]] in nearly all organisms. Glycolysis, through anaerobic respiration, is the main energy source in many [[prokaryotes]], [[eukaryotic]] cells devoid of [[mitochondria]] (e.g., mature [[erythrocytes]]) and eukaryotic cells under low-[[oxygen]] conditions (e.g., heavily-exercising muscle or fermenting [[yeast]]).
۳۰۹ کرښه:
[[Phosphofructokinase]] is an important control point in the glycolytic pathway, since it is one of the irreversible steps and has key allosteric effectors, [[AMP]] and [[fructose 1,6-bisphosphate]] (F1,6BP).
 
[[Fructose 2,6-bisphosphate]] (F2,6BP) is a very potent activator of phosphofructokinase (PFK-1) that is synthesised when F6P is phosphorylated by a second phosphofructokinase ([[PFK2]]). In liver, when blood sugar is low and [[glucagon]] elevates cAMP, [[PFK2]] is phosphorylated by protein kinase A. The phosphorylation inactivates [[PFK2]], and another domain on this protein becomes active as [[fructose 2,6-bisphosphatase]], which converts F2,6BP back to F6P. Both [[glucagon]] and [[epinephrine]] cause high levels of cAMP in the liver. The result of lower levels of liver fructose-2,6-bisphosphate is a decrease in activity of [[phosphofructokinase]] and an increase in activity of [[fructose 1,6-bisphosphatase]], so that gluconeogenesis (essentially "glycolysis in reverse") is favored. This is consistent with the role of the liver in such situations, since the response of the liver to these hormones is to release glucose to the blood.
 
[[Adenosine triphosphate|ATP]] competes with [[AMP]] for the allosteric effector site on the PFK enzyme. [[Adenosine triphosphate|ATP]] concentrations in cells are much higher than [[AMP]], typically 100-fold higher,<ref>Beis I., and Newsholme E. A. (1975). The contents of adenine nucleotides, phosphagens and some glycolytic intermediates in resting muscles from vertebrates and invertebrates. Biochem J 152, 23-32.</ref> but the concentration of [[Adenosine triphosphate|ATP]] does not change more than about 10% under physiological conditions, whereas a 10% drop in [[Adenosine triphosphate|ATP]] results in a 6-fold increase in [[AMP]].<ref>Voet D., and Voet J. G. (2004). Biochemistry 3rd Edition (New York, John Wiley & Sons, Inc.).</ref> Thus, the relevance of [[Adenosine triphosphate|ATP]] as an allosteric effector is questionable. An increase in [[AMP]] is a consequence of a decrease in [[energy charge]] in the cell.
 
[[Citrate]] inhibits phosphofructokinase when tested ''in vitro'' by enhancing the inhibitory effect of ATP. However, it is doubtful that this is a meaningful effect ''in vivo'', because citrate in the cytosol is mainly utilized for conversion to [[acetyl-CoA]] for [[fatty acid]] and [[cholesterol]] synthesis.
۳۴۳ کرښه:
* [[Pentose phosphate pathway]]
* [[Citric acid cycle]], which in turn leads to:
:* [[Amino acid synthesis]]
:* [[Nucleotide synthesis]]
:* [[Tetrapyrrole synthesis]]
 
From an energy perspective, NADH is either recycled to NAD+ during anaerobic conditions, to maintain the flux through the glycolytic pathway, or used during aerobic conditions to produce more ATP by [[oxidative phosphorylation]]. From an [[anabolism|anabolic]] metabolism perspective, the NADH has a role to drive synthetic reactions, doing so by directly or indirectly reducing the pool of NADP+ in the cell to NADPH, which is another important reducing agent for biosynthetic pathways in a cell.
۴۸۸ کرښه:
{{MetabolismMap}}
{{Glycolysis enzymes}}
{{Link FA|it}}
 
[[وېشنيزه:ژونکيميا]]
Line ۴۹۴ ⟶ ۴۹۳:
[[وېشنيزه:استقلابي لارې]]
[[وېشنيزه:کاربوهايډرېټ]]
 
{{Link FA|it}}
 
[[ar:تحلل سكري]]
Line ۵۲۶ ⟶ ۵۲۷:
[[pl:Glikoliza]]
[[pt:Glicólise]]
[[ro:GlicolizaGlicoliză]]
[[ru:Гликолиз]]
[[sl:Glikoliza]]