Life of bacteria Flashcards

(40 cards)

1
Q

Nutrition types of m.o.

A

two ways how to they obtain carbon and capture energy

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2
Q

autotrophy

A

self-feeding

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3
Q

heterotrophy

A

other-feeding

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4
Q

autotrophs use

A

carbon dioxide as a carbon source → synthesize organic molecules

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5
Q

photoautotrophs

A

energy from light by photosynthesis

- cyanobacteria

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6
Q

chemoautotrophs

A
  • energy from oxidizing simple inorganic substances such as sulfides and nitrites
  • nitrifying bacteria
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7
Q

heterotrophs

A
  • get carbon from ready-made organic molecules

- obtain from other organisms (dead or living)

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8
Q

chemoheterotrophs

A

chemical energy from breaking down ready-made organic compounds
(metatrophs + paratrophs)

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9
Q

metatrophs

A

obtain carbon from glycogen, starch and cellulose

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10
Q

paratrophs (parasites)

A

obtain carbon from soluble carbohydrates and nitrogen from AAs

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11
Q

photoheterotrophs

A

chemical energy from light to require organic substances as alcohols, fatty acids or carbohydrates as carbon sources

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12
Q

aerobes

A
  • require molecular oxygen for metabolism + growth
  • use oxygen for oxidation of nutrients and production of energy
  • final acceptor of electrons in ETC
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13
Q

anaerobes

A
  • dont require oxygen
  • oxygen = toxic
  • oxygen containing inorganic molecules (nitrates, nitrites) = final acceptors of electrons in ETC
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14
Q

facultative anaerobes

A
  • grow either in presence or absence of oxygen

- can generate ATP in aerobic and anaerobic conditions

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15
Q

microaerophiles

A
  • require oxygen in very low levels (2-10%)

- capnophiles → need elevated amount of carbon dioxide

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16
Q

bacterial enzymes are classified into

and subdivided into

A

→ endoenzymes intracellularly
→ exoenzymes secreted to environment
- subdivided into six groups acc. to catalyzed reactions

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17
Q

oxidoreductase

A
  • oxidation reduction reaction

- oxygen and hydrogen are added or released

18
Q

transferase

A
  • transfer specific functional groups (amine) from one molecule to another (alanine transaminase)
19
Q

hydrolase

A
  • participate in hydrolysis reactions (addition of water)
20
Q

lyase

A
  • transfer groups of atoms without hydrolysis reaction
21
Q

isomerase

A
  • reorganize atoms inside the molecule e.g. glucose phosphate isomerase
22
Q

ligase

A

join two large molecules by using ATP energy

23
Q

uptake of nutrients by the bacterial cell

A
  • passive diffusion

- active transport

24
Q

passive diffusion

A
  • concentration gradient of substances
  • transmembrane proteins (porins) form pores in membrane and cell wall
  • assist in transport function
  • pores + channels allow entry of ions and small hydrophilic molecules by passive diffusion
25
active transport
- against concentration gradient - permeases involved in a.t. - p. form phosphotransferase system → uses energy from high energy phosphoenolpyruvate molecules - PEP in cytoplasm → energy + phosphate group to a permease in membrane → transfers phosphate to sugar molecule and moves sugar across membrane - phosphorylated sugar is trasnported inside cell and prepared for metabolism
26
metabolism
- sum of all chemical processes which occur in the bacterial cell - consists of catabolism and anabolism
27
catabolism
chemical reactions that release energy by breaking complex molecules into simpler ones
28
anabolism
chemical reactions which require energy to synthesize complex molecules from simpler ones
29
catabolic reactions
- provide energy for bacteria that is required for bacterial life processes → movement, active transport of nutrients and synthesis of complex molecules - involve electron transfer → energy to be captured in high-energy bonds in ATP and similar molecules - ET = oxidation and reduction
30
anabolic reactions
- bacterial growth, reproduction and repair
31
energy production in bacteria
- in forms of ATP and NADH from glucose using 3 major pathways → glycolysis, TA cycle and PPP
32
glycolysis
- aerobic and anaerobic conditions | - yield 2 ATP, 2 NADH and 2 pyruvated molecules from 1 glucose molecule
33
main processes of glycolysis
1. substrate-level phosphorylation → transfer of P groups from ATP to glucose 2. breakdown of six-carbon glucose into 2 3-carbon molecules 3. transfer of 2 electrons to coenzyme NAD 4. capture of energy in ATP molecules
34
Krebs cycle
- acetyl groups are oxidized to carbon dioxide - hydrogen atoms are removed → electrons transferred to coenzymes (elec. carriers) - hydrogens combined with oxygen to form water - ONLY under aerobic conditions - more energy than from glycolysis - aerobic metabolism can produce 38 ATP molecules from glucose - 19 times more than anaerobic metabolism
35
main processes of krebs cycle
1. oxidation of carbon 2. transfer of electrons to coenzymes 3. capture of energy in ATP molecules
36
importance of TCA cycle
- most efficeint mechanism for ATP - final common pathway for complete oxidation of amino acids, fatty acids and carbohydrates - key intermediates for ultimate synthesis of AAs, lipids, purines and pyrimidines
37
PPP
- along with glycolysis - glucose and 5 carbon carbohydrates are brokes down - provide nucleic acid precursors and reducing power in form of NADPH - PPP → 1 ATP molecule for each oxidized glucose molecule
38
bacterial cell division
by binary fission
39
bacterial growth
- reproduce asexually → simple transverse binary fission - numbers increase logarithmically (n=2g) - rime for reprod. cycle = generation time → can vary - fast-growing bacteria have a generation time of 15-30min in vitro but more in vivo - obligate anaerobes grow much more slowly than aerobes → in vitro as well - tuberculosis bacs have an in vitro generation time of 12-24h - depends on nutrient content of medium
40
phases of bacterial growth
A. lag phase → adaptation of bacteria to medium → no division → increase in bacterial mass per unit of volume → no increase in cell count B. directly into c-phase C. division of bacteria fast → cell count increases logarithmically up to 10 hoch 9 /ml D. division slows down E. division slows down even more → nutrients already used → toxins → exhaustion of nutrients and increasing concentration of toxic metabolites F. bacs die