Quick viewing(Text Mode)

11-Major Metabolic Pathway TEAM436

11-Major Metabolic Pathway TEAM436

Major Metabolic Pathways of Glucose & Glucose Transport

– Color Index:

Important. §

Extra Information. § 436 Biochemistry team Doctors slides. § Objectives:

Define a metabolic pathway. Ø Describe the general metabolic pathways for Ø glucose (production and utilization). Ø Briefly describe the HMP. Ø Recognize the mechanisms of glucose transport Ø Pathway: Series of chemical reactions that have one goal. Reaction: Metabolic pathways Substrate+Substrate Product.

Definition

Pathway for glucose Site happens in almost every Regulatory mechanism(s) Reaction cell, starting by - Cellular tissue oxidation of glucose and 1- Rapid short-term Few are rate-limiting ending with pyruvate -Covalent modification (They are (tissue) (or lactate). -Allosteric found only in - Subcellular 2- Slow long-term irreversible Inside the cell (hormone) pathways). (Mitochondrial) -Induction\repression Metabolic pathways of glucose Catabolic Cycles Anabolic Cycles Production • & Gluconeogenesis Kreb (mainly) Glycogenesis • Glycogenolysis • HMP Glycogenolysis Gluco-neo- Hexose genesis interconversion To understand J *You DON’T have to know Catabolic Anabolic this*

Prefix: Glyco-: glucose Glycogeno-: glycogen *except in synthesis of glycogen: we say Utilization glycogensis instead of saying glycogeno-genesis. Hexose Glyco-lysis To differentiate: the HMP / PPP interconversion Glycogenesis Catabolic Catabolic Anabolic synthesis of glucose is glucoNEOgenesis*

Suffix: -genesis: process of producing Krebs cycle -lysis: breaking down. Catabolic *Aerobic: with oxygen *Anaerobic: without oxygen GLYCOLYSIS

u Oxidation (breaking down) of glucose to provide energy Aerobic glyclolysis Anaerobic Aerobic glycolysis glycolysis

When In absence of If there is oxygen , cells enough(adequate that lack supply) oxygen, mitochondria Cells that has mitochondria

End product Lactate + 2 ATP Pyruvate(s) + 8 ATP Glycogenesis and Glycogenolysis

Glycogenesis Glycogenolysis u Occurs when glucose and ATP are u Occurs in response to hormonal and present in relatively high amounts neural signals (This process is: storage) of glycogen into (ﺗﻜﺴﯿﺮ) u Degradation u Synthesis of glycogen from glucose glucose

(اذا زاد اﻟﺠﻠﻮﻛﻮز ﻓﻲ اﻟﺠﺴﻢ و ﻛﺎﻧﺖ ﻛﮫﺮﺑﺎﺋﯿﺔ او (اذا اﺣﺘﺎج اﻟﺠﺴﻢ ﻳﺮﺳﻞ اﺷﺎرت اﻟﻄﺎﻗﺔ ﻣﻮﺟﻮدة ﻳﺘﻢ ﺗﺨﺰﻳﻦ اﻟﺠﻠﻮﻛﻮز ﻋﻠﻰ ھﺮﻣﻮﻧﺎت ﻟﺘﻜﺴﯿﺮ اﻟﺠﻼﻳﻜﻮﺟﯿﻦ و ﺗﺤﻮﻳﻠﻪ ﺷﻜﻞ ﺟﻼﻳﻜﻮﺟﯿﻦ ﻋﺸﺎن ﻳﺤﺮﻗﻪ و ﻟﺠﻠﻮﻛﻮز) ﻳﺴﺘﺨﺪﻣﻪ ﺑﻌﺪﻳﻦ)

Both the same location: Mainly in and muscleà Cytosol Gluconeogenesis

ﺻﻨﺎﻋﺔ اﻟﺠﻠﻮﻛﻮز ﻣﻦ ﻣﻮاد ﻏﯿﺮ اﻟﻜﺮﺑﻮھﯿﺪرات u Synthesis of glucose from non- precursors Precursor: is a chemical that is transformed into another compound u The precursors could be lactate (anaerobic), pyruvate (aerobic), glycerol and alpha-keto u It requires mitochondria and cytosolic enzymes Glycerol: is a part of the triacylglycerol u Occurs in Liver and kidney molecule which is the main constituent of body fat.

Keto acids: are organic compounds that contain a carboxylic group and a group. The alpha-keto acids are especially important in biology as they are involved in the Krebs citric acid cycle and in glycolysis.

cytosolic enzymes: present in cytosol. Hexose MonoPhosphate shunt (HMP) Note: Oxidation of glucose, also Also known as Pathway (PPP) known as glycolysis, is the process which releases energy stored in glucose by combining it with u HMP shunt is an alternative (another) pathway of glucose oxidation. oxygen. u Has the same regulatory mechanism's as glucose (rapid short-term and slow long-term) u it is not involved in the generation of energy unlike glycolysis u Around 10% of glucose (that all the body makes) is entered in this pathway. ﻓﯿﺪﻳﻮ ﻳﻠ ّﺨﺺ u In liver and kidneyà this percentage is up to 30% ﻟﻚ u Occurs in many places such as the cytosol of the liver, adipose tissue (to produce fatty acids from glucose) u Has two main functions and two phases 1- Oxidative phase 2- Non-oxidative phase

1-Provides NADPH 2- Provides Biomedical Importance of (HMP) & (PPP)

A source of NADPH NADPH is required for: 1. Synthesis of fattyacids, and some Provides Pentoses for: (Pentose and its amino acids. derivatives are useful in the synthesis of: ) 2. Detoxification of drugs by (cytochrome 1. Nucleic acids (DNA and RNA ) P450 ) . 2. Nucleotides ( ATP , NAD ,FAD and CoA ) 3. In scavenging (remove) the free radicals .

Note: Cytochrome P450: enzymes also function to metabolize potentially toxic compounds, including drugs and products of endogenous such as bilirubin 436 Biochemistry team From Lippincott Tissue Distribution

Location of HMP: in the Cytosol of the following locations:

Liver Lactating Adrenal cortex Gonads mammary glands Adipose Tissue Erythrocytes(RBC) Lens Cornea to reduce Notes J Glutathione: antioxidant capable of preventing Phases of HMP Shunt damage caused by . (Free Radicals) Cornea: the transparent layer forming the front of the eye. Non-Oxidative phase The adrenal cortex: the Oxidative phase -which provides outer part of the adrenal -which provides NADPH- gland. pentoses- Gonads: an organ that produces gametes; a testis or Oxidative phase 436 Biochemistry team Non-Oxidative phase ovary. Colors are for your understanding J Phase1: oxidative pathway

The purpose of this phase is to :

1- provide 2 NADPH

2- convert Glucose6-phosphate to Ribulose 5-phospate which is an important molecule to start the next phase.

Note J We start with Glucose-6-Phosphate C6H13O9P We end with Ribulose 5-phosphate C5H11O8P

Ribose: sugar Ribulose: Ketone sugar Phase2: non oxidative ***girls doctor said skip it A) Interconversion of pentose اﻟﮫﺪف ﻣﻨﻪ ﺳﻜﺮ ﺧﻤﺎﺳﻲ u Ribulose 5 phosphate Xylulose-5P: an intermediate in the وﺳﺪاﺳﻲ pentose phosphate :ﻳﺘﺤﻮل اﻟﻰ u pathway. It is a u 5 phosphate sugar formed from ribulose-5- phosphate. These non-oxidative reversible reactions permit ribulose 5-phosphate to be converted either to ribose 5-phosphate (needed for nucleotide synthesis) or to intermediates of glycolysis— 6- #ﻟﻠرﺑط: ﺗﻧطق "زي اﻟﻠوز" phosphate ّ *** .and glyceraldehyde 3-phosphate

Remember that 2 important enzymes are needed in non-oxidative reactions :

• 1- , an always associated with TPP ( pyrophosphate) •TPP: a prosthetic group (is a Coenzyme associated permanently) for the Transketolase enzyme. • It is important to activate the enzyme.

• 2- . Non Oxidative اﻟﺘﻔﺎﻋﻞ اﻻول Colors are for your (Conversion of pentose ﺗﺤﻮﻳﻞ ribulose اﻟﻰ phosphate to hexose ribose understanding J phosphate) اﻟﺘﻔﺎﻋﻞ اﻟﺜﺎﻧﻲ Ribose + xylulose ( this reaction is ﻣﮫﻢ catalyzed by Transketolase with TPP). And will give us 2 new sugar molecules : Sedoheptolose (7C) AND glyceraldehyde (3C)

اﻟﺘﻔﺎﻋﻞ اﻟﺜﺎﻟﺚ

Sedoheptolose +glyceraldehyde (this reaction is catalyzed by Transaldolase) And will give us 2 new sugar molecules : fructose (6C). And erythrose (4C).

اﻟﺘﻔﺎﻋﻞ اﻷﺧﯿﺮ ﺗﻔﺎﻋﻼت Xylulose ﺗﻜﻮن ﻣﺼﺤﻮﺑﺔ ﺑﺈﻧﺰﻳﻢ Xylulose5-P+Erythrose4-P ( this transketolase . reaction is catalyzed by وزي ﻣﺎﻗﻠﻨﺎ ھﺎﻹﻧﺰﻳﻢ Transketolase with TPP. And will give داﻳﻤﺎ ﻳﻜﻮن ﻣﻌﺎه Note: both Glyceraldehyde TPP and fructose are us 2 sugar molecules : Fructose 6-P AND intermediates of glycolysis Glyceraldehyde 3-P . Colors are for your understanding J

Phase One Phase One

Enzymes numbered above are: 1, 2) glucose 6-phosphate dehydrogenase and 6-phosphogluconolactone 3) 6-phosphogluconate dehydrogenase, 4) ribose 5-phosphate , 5) 6 and 8) transketolase (coenzyme: ) and 7) transaldolase. Extra explanation: From Lippincott Clinical Correlations G-6-PD deficiency results in :

Notes J Glucose-6-phosphate dehydrogenase Heamolytic Aneamia deficiency The condition is characterized by abnormally low levels of glucose-6- phosphate dehydrogenase, an enzyme involved in the pentose phosphate pathway that is especially important in Neonatal the . G6PD deficiency is the most common human enzyme Jaundice defect Hemolytic anemia: relating to or involving the rupture or destruction of red blood cells. Neonata: relating to newborn children Kidney failure • Tissue-specific expression Glucose Transport (GLUT 1-14) pattern

Na+ 1. GLUT-1 RBCs and brain (blood-brain Co- Na-Independent Facilitated Diffusion barrier) transporter: 2. GLUT-2 Liver, kidney & pancreas

1. Against 1. Down the 3. GLUT-3 Neurons concentration concentration gradient gradient 2. Energy 2. Energy- 4. GLUT-4 Adipose tissue & skeletal dependent Independent muscle 5. GLUT-5 3. Carrier-mediated 3. Glucose Small intestine & testes 4. Coupled to Na+ Transporters transport (GLUT 1-14) 6. GLUT-7 Liver (ER-membrane

Boys doctor mentioned that GLUT-1, 3 & 4: Uptake of glucose from the blood. now it 20 Glucose transporters GLUT-2: Blood, cells it’s a bidirectional transporter, Note : GLUT-4 is insulin allowing glucose to flow in 2 directions. sensitive, because it GLUT-5: Fructose transport . needs insulin to work. Glucose Transport: Facilitated Diffusion

435 Teamwork: - اﻟﺠﻠﻮﻛﻮز ﻻ ﻳﺴﺘﻄﯿﻊ أن ﻳﻨﺘﺸﺮ ﺧﻼل اﻟﺨﻠﯿﺔ , ﻷﻧﻪ ﻣﺮﻛﺐ ھﺎﻳﺪروﻓﯿﻠﻚ \ ﻣﺤﺐ ﻟﻠﻤﺎء . - ﻟﺬﻟﻚ ﻓﮫﻮ ﻳﺤﺘﺎج إﻟﻰ طﺮﻳﻘﺔ أﺧﺮى , ﻓﺈﻣﺎ أن ﻳﺪﺧﻞ ﻣﻊ اﻟﺼﻮدﻳﻮم ﻋﻦ طﺮﻳﻖ اﻟﻜﻮ ﺗﺮاﻧﺴﺒﻮرت اﻟﺬي ﺳﺒﻖ أن ﺗﻌﺮﻓﻨﺎ ﻋﻠﯿﻪ ﺑﺎﻟﻔﺴﯿﻮﻟﻮﺟﻲ. - أو أﻧﻪ ﻳﺪﺧﻞ ﻋﻦ طﺮﻳﻖ ﻛﺎرﻳﺮ ﺑﺮوﺗﯿﻨﺰ ﺧﺎﺻﺔ ﺑﻪ ﺑﻄﺮﻳﻘﺔ اﻟﻔﺎﺳﯿﻠﯿﺘﺪ دﻓﯿﻮﺟﻦ واﻟﺘﻲ أﻳﻀﺎ ﺳﺒﻖ اﻟﺘﻌﺮف ﻋﻠﯿﮫﺎ ﺑﺎﻟﻔﺴﯿﻮﻟﻮﺟﻲ. (ﻣﺜﻞ اﻟﺼﻮرة) Revision Take home messages u There are multiple pathways for glucose that can be grouped in to catabolic (utilizing glucose) or anabolic (producing glucose) u Glycolysis is the major metabolic pathway of glucose breakdown to provide energy u Alternative pathway for glucose oxidation but not meant for producing energy u Has two phases- oxidative and non-oxidative u During oxidative phase, glucose-6-P is oxidized with generation of 2 moles of NADPH, and one mole of pentose phosphate, with liberation of CO2 u During non-oxidative phase, pentose phosphate is converted to intermediates of glycolysis QUIZ u Boys team members:

1- ﺣﻤﺪ اﻟﺤﺴﻮن. 2- ﻣﺤﻤﺪ ﺣﻜﻤﻲ. 3- ﺧﺎﻟﺪ اﻟﻘﺤﻄﺎﻧﻲ. :u Girls team members 4- ﺣﻤﺪ اﻟﺤﻤﯿﺪان. 5- ﻣﺤﻤﺪ ﺣﺒﯿﺐ. ﻧﻮرة اﻟﺸﺒﯿﺐ 6- ﺧﺎﻟﺪ اﻟﺮاﺟﺢ. 7- ﻓﮫﺪ اﻟﻌﺘﯿﺒﻲ. 8- طﻼل اﻟﻄﺨﯿﻢ.

-Team leaders: ﻋﺒﺪﷲ اﻟﻤﺎﻧﻊ. :Contact us- ﻧﻮره اﻟﺴﮫﻠﻲ. [email protected]

twitter.com/436biochemteam