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BIO-310 BIOCHEMISTRY II

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BIO-310

BIOCHEMISTRY II

VI. WEEK

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LECTURE CONTENTS OF 6TH WEEK

Net reaction of β-oxidation of saturated fatty acids, calculation of energy balance

Oxidation of unsaturated fatty acids:

Monounsaturated, Polyunsaturated

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https://www.google.com/url?sa=i&url=https%3A%2F%2Fpharmaxchange.info%2F2013%2F10%2Foxidation-of- unsaturated-fatty-acids

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https://www.google.com/url?sa=i&url=https%3A%2F%2Fpharmaxchange.info%2F2013%2F10%2Foxidation-of- unsaturated-fatty-acids

%2F&psig=AOvVaw2sHGYC0fi6kmudXCS1M2mI&ust=1589318355084000&source=images&cd=vfe&ved=0CAIQj RxqFwoTCPDNkbTerOkCFQAAAAAdAAAAABAD

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Malonil-CoA formation

Β-oxidation in peroxisome and glioxisome

Ω-oxidation

Ketone Bodies

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In the β-oxidation of saturated fatty acids, formation of acetyl-KoA occurs with acyl-CoA dehydrogenase (FAD is reduced) in the first step, enoyl-CoA hydratase in the second step (double bond impregnation), β-hydroxyachyl-CoA dehydrogenase in the third step (reduction of NAD), and with the thiolase enzyme in the final step.

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Oxidation of unsaturated fatty acids;

In monounsaturated fatty acids, reactions with additional enoyl-KoA isomerase enzyme and β- oxidation enzymes are completed.

In the case of polyunsaturated fatty acids, energy is produced by additional isomerase, reductase and isomerase enzymes.

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https://www.google.com/url?sa=i&url=http%3A%2F%2Fwww.bioinfo.org.cn%2Fbook%2Fbiochemistry

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Oxidation of fatty acids in the mitochondria should be checked if the energy from the fatty acids is

not needed by the cell. The first of these is malonyl-KoA formation.

Malonyl-CoA is synthesized starting from acetyl- CoA in the cytoplasm. This molecule is a molecule that stimulates the synthesis of fatty acids.

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https://www.google.com/url?sa=i&url=https%3A%2F%2Fslideplayer.com%2Fslide

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https://www.google.com/url?sa=i&url=https%3A%2F%2Fwww.memorangapp.com%2Fflashcards%2F126075%2FOxidation

%2Bof%2BFatty%2BAcids%2Band%2BKetones

%2F&psig=AOvVaw0JgA0OUNnCTODREtg55Yke&ust=1589318494728000&source=images&cd=vfe&ved=0CAIQjRxqFwo TCLjMiPrerOkCFQAAAAAdAAAAABA-

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When the ratio of NADH / NAD + concentrations in mitochondria is high, the activity of β-hydroxyacyl- CoA dehydrogenase decreases.

Increasing the concentration of acetyl-CoA inhibits thiolase.

These allow the regulation of mitochondrial β- oxidation of fatty acids.

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The difference of β-oxidation in peroxisome and glioxisome from mitochondria is transportation of the hydrogen peroxide formed in the first step and NADH formed in the oxidative stage at the peroxisome and glioksizom, to the cytoplasm without re-oxidized.

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https://www.google.com/url?sa=i&url=http%3A%2F%2Fwww.bioinfo.org.cn%2Fbook%2Fbiochemistry

%2Fchapt16%2Fbio3.htm&psig=AOvVaw1nHj1NScsde9h_4D7sCaEc&ust=1589318746460000&source=image s&cd=vfe&ved=0CAIQjRxqFwoTCMCjlO7frOkCFQAAAAAdAAAAABAD

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https://www.google.com/url?sa=i&url=https%3A%2F%2Fslideplayer.com%2Fslide

%2F10338735%2F&psig=AOvVaw2ObXYiUVZkXL_6EVw0AGRT&ust=1589318896302000&source=images&cd=vfe&ve d=0CAIQjRxqFwoTCNjsmLfgrOkCFQAAAAAdAAAAABAT

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Apart from β-oxidation, Ω-oxidation of fatty acids is also available.

The Ω-oxidation takes place in the endoplasmic reticulum as an alternative to mitochondridia.

10 or 12 C fatty acids are used here

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Mixed-function oxidases, alcohol dehydrogenase, and aldehyde dehydrogenase are used in Ω-

oxidation.

Beta oxidation occurs at both ends.

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Acetyl-CoA formed by oxidation of fatty acids in many mammalian cells can enter the citric acid cycle or turn into ketone bodies such as acetone, acetoacetate, β-hydroxybutyrate to be transported to other tissues.

High concentrations cause acidosis and ketosis

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https://www.google.com/url?sa=i&url=https%3A%2F%2Fwww.slideshare.net%2FKamleshYadav35%2Fketone-bodi

es-78734577&psig=AOvVaw2RVRqMtFYuzWaG1hzyI29s&ust=1589138417063000&source=images&cd=vfe&ved=0CAIQjR xqFwoTCPCajcXAp-kCFQAAAAAdAAAAABA3

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https://www.google.com/url?sa=i&url=https%3A%2F%2Fwww.researchgate.net%2Ffigure%2FProduction-of-ketones-and-energy- production-Ketone-bodies-namely-acetoacetate-

acetone_fig2_306274211&psig=AOvVaw2RVRqMtFYuzWaG1hzyI29s&ust=1589138417063000&source=images&cd=vfe&ved=0 CAIQjRxqFwoTCPCajcXAp-kCFQAAAAAdAAAAABA8

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BIOCHEMICAL FORMULAS WILL BE DISCUSSED WITH IN THIS

SECTION

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REFERENCES

MAIN : LEHNINGER PRINCIPLES OF BIOCHEMISTRY, DAVID L. NELSON, MICHAEL M.

COX, 5TH EDITION, 2013.

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PRİNCİPLES OF BİOCHEMİSTRY, H. R. HORTON, L.

A. MORAN, K. G. SCRİMGEOUR, M. D. PERRY, J.

D. RAWN, PEARSON PRENTİS HALL, 2006.

COLOR ATLAS OF BIOCHEMISTRY, J. KOOLMAN, K. H. ROEHM, GEORG THIEME VERLAG, 2005.

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HARPER’S ILLUSTRATED BIOCHEMISTRY, R. K.

MURRAY, D. K. GRANNER, P. A. MAYES, V. W.

RODWELL, LANGE MEDICAL BOOKS/MCGRAW- HİLL MEDICAL PUBLISHING DIVISION, 2003.

BASİC CONCEPTS İN BİOCHEMİSTRY, A STUDENT’S SURVİVAL GUİDE, H. F. GİLBERT, MCGRAW-HİLL HEALTH PROFFESİONS DİVİSİON, 2000.

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HARPER’S ILLUSTRATED BIOCHEMISTRY, R. K.

MURRAY, D. K. GRANNER, P. A. MAYES, V. W.

RODWELL, LANGE MEDICAL BOOKS/MCGRAW- HİLL MEDICAL PUBLISHING DIVISION, 2003.

BASİC CONCEPTS İN BİOCHEMİSTRY, A STUDENT’S SURVİVAL GUİDE, H. F. GİLBERT, MCGRAW-HİLL HEALTH PROFFESİONS DİVİSİON, 2000.

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