Lecture 2 - Plasma membrane Flashcards

1
Q

Give 4 reasons why bacterial physiology is used

A
  1. Explains ubiquity and success = evolution, survival, adaptation
  2. Explains beneficial and detrimental effects
  3. Insight into life and evolution ie expression of genome
  4. Strategic dvlpmt of antibacterials
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2
Q

List the 5 components of the bacterial cell envelope

A
  1. Plasma membrane (PM) = all
  2. Cell wall (CW) = most
  3. Outer membrane (OM) = some
  4. Periplasmic space (P) = some
  5. Flagella, pili, fimbriae, capsules, S layers = some
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3
Q

What are the 7 functions of the cell envelope?

A
  1. Rigidity and structure
  2. Prevent osmotic lysis
  3. Encloses contents
  4. Interact with external environ
  5. Receptors to respond to external environ
  6. Motility and attachment
  7. Critical to evolution eg monoderms or diderms 1st unknown
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4
Q

Describe bacterial lipids incl hopanoids and how they differ from eukaryotic lipids

A
  • Differ bc no sterols/cholesterol except mycoplasma
  • Hopanoids = sterol-like molecules that stabilise membrane and increase survival under stress
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5
Q

Describe the 2 types of proteins

A
  1. Peripheral (20-30%) = loosely connected, easy removal, water soluble
  2. Integral (70-80%) = not easily removed, insoluble, amphipathic
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6
Q

Define the fluid mosaic model and the current evidence against it

A
  • Proteins float in homogenously distributed lipids, move laterally
  • Functional membrane microdomains (FFMs) with unique integral flotillins = assemble protein complexes for specific processes
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7
Q

Describe the function of the PM as a selectively permeable osmotic barrier

A

Retain contents and prevent leakage

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8
Q

Describe the 2 functions of the PM controlling movement of chemicals

A
  1. Passive barrier to polar, charged, large
  2. Transport systems for uptake, excretion, secretion
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9
Q

List the 7 cellular processes that the PM functions as a site of

A
  1. Assembly and synthesis of lipids/proteins
  2. Assembly and secretion of extracellular proteins
  3. Enzymes
  4. Energy generation
  5. Receptor molecules
  6. Motility
  7. Chromosome attachment and separation
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10
Q

Describe passive diffusion - energy requirements, conc grad, types of molecules

A
  • No energy
  • Down conc grad, rate depends on size
  • Small, neutral, weakly charged
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11
Q

Describe facilitated diffusion - energy requirements, conc grad, 2 transport proteins, conc grad

A
  • No energy
  • Channel proteins = pores; carrier proteins/permeases that change conformation
  • Down conc grad till equal, depends on size, faster than passive
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12
Q

Describe overall active transport - energy, conc grad, proteins

A
  • ATP or proton motive force energy
  • Against conc grad
  • Permeases and peripheral substrate binding proteins
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13
Q

Describe primary active transport - transporter, type of transporter, modifications

A
  • ATP binding cassette (ABC) transporters
  • Uniporter
  • No mods to substance
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14
Q

What is the 3 step process of primary active transport?

A
  1. Solute binding protein binds substrate, attaches to transporter
  2. ATP hydrolysis releases energy at transport complex
  3. Substrate transported thru pore
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15
Q

Describe secondary active transport - energy source, modifications, type of transporter and subtypes

A
  • Potential energy from ion gradiens
  • No mods
  • Cotransporters = 2 substances incl ion
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16
Q

What are the 3 types of cotransporters and give an example of each

A
  1. Symporters = same direction eg H+ and solute
  2. Antiporters = opposite directions eg H+ in solute/Na+ out
17
Q

Describe group translocation active transport - solutes, type of transporter, mods, system used

A
  • Glucose and mannitol
  • Uniporter
  • Chemically mods = uptake when membrane de-energised
  • Sugar phosphotransferase system (PTS) or phosphorelay system
18
Q

Describe the 4 step process of the sugar phosphotransferase system (PTS)

A
  1. Phosphoenolpyruvate (PEP) donates phosphate to enzyme 1
  2. E1 donates to heat stable protein HPr
  3. HPR donates to E2a to E2b
  4. E2b translocates and phosphorylates sugar across using E2c permease