MCB 229 Spring 2000 Study Guide 5 Prof.
Terry
Covers Lecture for Feb. 15
This study guide is intended for you to use while you are
doing the assigned text reading. Quiz questions will be made with reference to
topics in this study guide. Quiz #5, based on questions from this study guide,
must be completed by midnight before the class on Tuesday, Feb. 15. You will
need to create your "myWebCT" account and visit the MCB 229 WebCT page in order
to access this quiz.
Chapter 7
- What do the following terms mean? Sterilize, disinfect, sanitize,
pasteurize, antiseptic, disinfectant, germicide, bactericide, fungicide?
What’s the difference between a bactericidal and bacteriostatic
agent?
- Does the population size matter when estimating how long to treat a
microbial sample to achieve sterility? If so, why?
- If 70% ethanol is good,
95% ethanol is better as an antimicrobial, right? Explain.
- Fruits and
tomatoes can be pasteurized more rapidly than milk. Why?
- Does organic
matter in water affect the level of disinfectant required to reach acceptable
levels? Why?
- What procedures are best used to sterilize liquid samples? Dry
glassware? Heat-sensitive solutions?
- Does the “thermal death
time” (TDT) tell you exactly how long you need to heat a sample to achieve
sterility? If not, what does it tell you?
- What does “decimal reduction
time” (D) measure? If you have a sample of 109 bacteria, and D
for this organism is 0.5 min, how long will you have to treat in order to get
reduce the population theoretically to 1 organism
(10o)?
- It’s Thanksgiving and you’ve served up the
turkey with stuffing at noon. By 6 p.m. the stuffing has become an incubator
for S. aureus, and the bacterial population has grown to 104
bacteria/gm. You want to snack later on, and you put the stuffing in a warm oven
at 60°C to warm up and, you hope, kill bacteria. How long should you wait
to eat the turkey, if you want to reduce the bacterial count to no more than 1
bacterium/gm (10o)? The D60 for Staphylococcus
aureus in turkey stuffing is 15.4 minutes.
- Skim details of autoclaving,
pp. 140-141.
- How do depth filters and membrane filters differ? Where would
you find a HEPA filter?
- Are there any microorganisms that would not be
removed from a solution by filtering through a 0.2 micrometer membrane
filter?
- What are the advantages and disadvantages of using UV and ionizing
radiation as sterilizing agents?
- Note that the distinction between
disinfectants and antiseptics is often fuzzy. Some chemicals such as ethanol can
be used for either purpose; in other cases the same chemical may be diluted when
used as an antiseptic, relative to its concentration when used as a
disinfectant.
- Look at Table 7.4. Which compounds have the highest activity?
Moderate activity? Low activity? Don’t memorize these, just get a sense of
the variation in effects.
- What are “phenolics”? Where are they
routinely used?
- How does each of the following work (i.e., what is their
cellular target): alcohols, iodine and chlorine (halogens), heavy metals,
detergents, aldehydes.
- What is the phenol coefficient test? What is it used
for?
Chapter 8
- Examine the structure of ATP (Fig. 8.2). There are a few chemicals you
should be able to recognize at sight – this is one! ATP hydrolysis is
coupled to many cellular reactions, releasing sufficient energy to make these
reactions occur spontaneously.
- What are the 1st and
2nd laws of thermodynamics? (Easy mnemonics: law 1 = “you
can’t get out of the ball game”, law 2 = “you can’t
win”).
- ΔG is a potentially confusing
concept. It is more useful than ΔH, the
difference in heat energy, because ΔG measures
the available energy (after accounting for entropy, which does not contribute to
useful work). We won’t do any calculations, so don’t worry about the
mathematical symbolism here. But we need to know the difference between
ΔG and
ΔGo'. The former is defined in terms
of actual concentrations of reactants and products, which change; the latter is
calculated based on standard concentrations.
ΔGo' values give a first
approximation to the magnitude of free energy change involved in a reaction,
including a prediction of whether the reaction is endergonic or exergonic.
- What characteristics would you expect of a chemical reaction with a
ΔGo' of +15 kcal/mole? Of – 0.1
kcal/mole? Of – 54 kcal/mole?
- How can you recognize an oxidation
reaction? A reduction reaction? Do these two always occur together?
- What
does NAD stand for? Be able to recognize this molecule from its structural
formula (Fig. 8.8). Compare this with the diagram of ATP so you don’t get
confused. Note that NAD+ includes and ADP molecule as part of its structure,
along with an additional ribose and a nicotinamide group.
- What is the
difference between NAD+ and NADH? Is the total amount of (NAD+ and NADH) in a
cell very small, very large, or somewhere in between?
- How does NADP differ
from NAD? (See legend to Figure 8.8a, and look closely at the figure). Note that
NAD is used primarily in reactions in which molecules are broken down
(catabolism), while NADP is used primarily in reactions where molecules are
being built up (anabolism). More to come on this as we explore Chapters 9 and
10.
- In addition to NAD and NADP, you should be able to recognize two other
very common redox carriers: FAD (see Fig. 8.9) and heme (Fig. 8.11). We’ll
see more of these in Ch. 9.
- What is an enzyme? How is an enzyme different
from a catalyst? What is the difference between the following terms: apoenzyme,
cofactor, holoenzyme, prosthetic group, coenzyme?
- Do enzymes affect the
overall energy change of a reaction? The rate of a reaction? The activation
energy of a reaction? (give a yes or no for each of these).
- What is the
active site of an enzyme? What happens there?
- What happens to the active
site when an enzyme is denatured? Is the protein chain broken into smaller
pieces during such a process?
- What is the difference between a competitive
and noncompetitive inhibitor? In which category would you place a chemical that
closely resembles the ordinary substrate? A heavy metal?