pharmaceutics

44
Foundations in Microbiology Chapter 8 PowerPoint to accompany Fifth Edition Talaro Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

Upload: umair-hanif

Post on 16-Apr-2017

1.569 views

Category:

Education


0 download

TRANSCRIPT

Page 1: pharmaceutics

Foundations in Microbiology

Chapter8

PowerPoint to accompany

Fifth Edition

Talaro

Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.

Page 2: pharmaceutics

Microbial Metabolism: The Chemical Crossroads of Life

Chapter 8

Page 3: pharmaceutics

Metabolism

The sum total of all chemical reactions & physical workings

occurring in a cell

Page 4: pharmaceutics

4

2 types of metabolism

• Anabolism - biosynthesis– building complex molecules from simple ones– requires energy (ATP)

• Catabolism - degradation– breaking down complex molecules into simple

ones– generates energy (ATP)

Page 5: pharmaceutics

5

Page 6: pharmaceutics

6

Page 7: pharmaceutics

7

Page 8: pharmaceutics

8

Enzyme structure

• Simple enzymes – consist of protein alone• Conjugated enzymes or holoenzymes –

contain protein and nonprotein molecules– apoenzyme –protein portion– cofactors – nonprotein portion

• metallic cofactors – iron, copper, magnesium • coenzymes -organic molecules - vitamins

Page 9: pharmaceutics

9

Page 10: pharmaceutics

10

Enzyme-substrate interactions

Page 11: pharmaceutics

11

• Exoenzymes – transported extracellularly, where they break down large food molecules or harmful chemicals; cellulase, amylase, penicillinase

• Endoenzymes – retained intracellularly & function there

Page 12: pharmaceutics

12

Page 13: pharmaceutics

13

• Constitutive enzymes – always present, always produced in equal amounts or at equal rates, regardless of amount of substrate; enzymes involved in glucose metabolism

• Induced enzymes – not constantly present, produced only when substrate is present, prevents cell from wasting resources

Page 14: pharmaceutics

14

Page 15: pharmaceutics

15

• Synthesis or condensation reactions – anabolic reactions to form covalent bonds between smaller substrate molecules, require ATP, release one molecule of water for each bond

• Hydrolysis reactions– catabolic reactions that break down substrates into small molecules, requires the input of water

Page 16: pharmaceutics

16

Page 17: pharmaceutics

17

Transfer reactions by enzymes

1. Oxidation-reduction reactions – transfer of electrons

2. Aminotransferases – convert one type of amino acid to another by transferring an amino group

3. Phosphotransferases – transfer phosphate groups, involved in energy transfer

4. Methyltransferases – move methyl groups from one molecule to another

5. Decarboxylases – remove carbon dioxide from organic acids

Page 18: pharmaceutics

18

Metabolic pathways

Page 19: pharmaceutics

19

Control of enzyme activity

1. Competitive inhibition – substance that resembles normal substrate competes with substrate for active site

2. Feedback inhibition – concentration of product at the end of a pathway blocks the action of a key enzyme

3. Feedback repression – inhibits at the genetic level by controlling synthesis of key enzymes

4. Enzyme induction – enzymes are made only when suitable substrates are present

Page 20: pharmaceutics

20

Competitive inhibition

Page 21: pharmaceutics

21

Energy –capacity to do work or cause change

• Endergonic reactions – consume energy• Exergonic reactions – release energy

Page 22: pharmaceutics

22

Redox reactions

• always occur in pairs• There is an electron donor and electron

acceptor which constitute a redox pair• The process salvages electrons & their

energy.• released energy can be captured to

phosphorylate ADP or another compound

Page 23: pharmaceutics

23

Electron carriers

• resemble shuttles that are loaded and unloaded with electrons and hydrogen

• most carriers are coenzymes, NAD, FAD, NADP, coenzyme A & compounds of the respiratory chain

Page 24: pharmaceutics

24

NAD reduction

Page 25: pharmaceutics

25

Electron carriers

Page 26: pharmaceutics

26

ATP

• 3 part molecule consisting of– adenine – a nitrogenous base– ribose – a 5-carbon sugar– 3 phosphate groups

• Removal of the terminal phosphate releases energy

Page 27: pharmaceutics

27

ATP

Page 28: pharmaceutics

28

Phosphorylation of glucose by ATP

Page 29: pharmaceutics

29

Formation of ATP

1. substrate-level phosphorylation2. oxidative phosphorylation3. photophosphorylation

Page 30: pharmaceutics

30

substrate-level phosphorylation

Page 31: pharmaceutics

31

Catabolism of glucose

1. Glycolysis2. Tricarboxylic acid cycle, Kreb’s cycle3. Respiratory chain, electron transport

Page 32: pharmaceutics

32

Metabolic strategies

Pathwaysinvolved

Final e- acceptor ATP yield

Aerobic respiration

Glycolysis, TCA, ET

O2 38

Anaerobic respiration

Glycolysis, TCA, ET

NO3-, So4

-2, CO3

-3

variable

Fermentation Glycolysis Organic molecules

2

Page 33: pharmaceutics

33

Overview of aerobic respiration

Page 34: pharmaceutics

34

Overview of aerobic respiration

• Glycolysis – glucose (6C) is oxidized and split into 2 molecules of pyruvic acid (3C)

• TCA – processes pyruvic acid and generates 3 CO2 molecules

• Electron transport chain – accepts electrons NADH & FADH, generates energy through sequential redox reactions called oxidative phosphorylation

Page 35: pharmaceutics

35

Glycolysis

Page 36: pharmaceutics

36

TCA cycle

Page 37: pharmaceutics

37

Electron transport system

Page 38: pharmaceutics

38

Chemiosmosis

Page 39: pharmaceutics

39

Fermentation

• Incomplete oxidation of glucose or other carbohydrates in the absence of oxygen

• Uses organic compounds as terminal electron acceptors

• Yields a small amount of ATP• Production of ethyl alcohol by yeasts acting on

glucose• Formation of acid, gas & other products by the

action of various bacteria on pyruvic acid

Page 40: pharmaceutics

40

Fermentation

Page 41: pharmaceutics

41

Products of fermentation

Page 42: pharmaceutics

42

• Many pathways of metabolism are bi-directional or amphibolic

• Metabolites can serve as building blocks or sources of energy– Pyruvic acid can be converted into amino acids through

amination– Amino acids can be converted into energy sources

through deamination– Glyceraldehyde-3-phosphate can be converted into

precursors for amino acids, carbohydrates and fats

Page 43: pharmaceutics

43

Page 44: pharmaceutics

44