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Imagine that you were working with Monod and Jacob to find mutants that can't grow using lactose. After treating cells with a mutagen, you anticipate a mutation rate of \(1 \times 10^{-4}\) lactosenonutilizing mutations per cell. Based on this estimate, how many cells should you screen to have a good chance of finding one mutant?

Short Answer

Expert verified
To have at least a 95% chance of finding at least one lactose non-utilizing mutant, you should screen approximately 2996 cells.

Step by step solution

01

Find the probability of finding a mutant in a single cell

The given mutation rate is \(1 \times 10^{-4}\) lactosenonutilizing mutations per cell, which means that the probability of finding a mutant in a single cell is \(1 \times 10^{-4}\), or 0.0001.
02

Find the probability of not finding a mutant in a single cell

The probability of not finding a mutant in a single cell is the complement of the probability of finding a mutant. This can be calculated as: \[P(\text{not a mutant}) = 1 - P(\text{mutant})\] \[P(\text{not a mutant}) = 1 - 0.0001\] \[P(\text{not a mutant}) = 0.9999\]
03

Calculate the probability of not finding a mutant in n cells

To find the probability of not finding a mutant after screening n cells, we can multiply the probability of not finding a mutant in each cell. Using the probability calculated in Step 2: \[P(\text{no mutant in n cells}) = (0.9999)^n\]
04

Find the probability of finding at least one mutant in n cells

The probability of finding at least one mutant after screening n cells is the complement of the probability of not finding any mutant at all, which can be calculated as: \[P(\text{at least one mutant}) = 1 - P(\text{no mutant in n cells})\] \[P(\text{at least one mutant}) = 1 - (0.9999)^n\]
05

Determine the desired probability and solve for n

Let's say we want to have at least a 95% chance (0.95 probability) of finding a mutant. We can set the probability calculated in Step 4 equal to 0.95 and solve for n: \[0.95 = 1 - (0.9999)^n\] \[0.05 = (0.9999)^n\] To solve for n, we can take the natural logarithm of both sides: \[\ln(0.05) = n \ln(0.9999)\] Now we can solve for n: \[n = \frac{\ln(0.05)}{\ln(0.9999)} ≈ 2995.5\]
06

Round up the number of cells to screen

Since we cannot screen a fraction of a cell, we need to round up the number of cells to screen. In this case, we should screen at least 2996 cells to have a good chance (95% probability) of finding at least one mutant.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Probability of Mutation
Understanding the probability of mutation is essential when working in genetics, particularly when studying mutation rates. Mutations are changes in the DNA sequence, which occur at different rates depending on environmental factors and the organism itself.
In this context, the mutation rate indicates how likely it is for a genetic mutation to occur in a single cell.
For the scenario we're looking at, the mutation rate for lactose nonutilizing mutants is given as \(1 \times 10^{-4}\).
This means for every single cell observed, there's a 0.0001 probability—or 0.01% chance—of detecting a mutant. Calculating and understanding the mutation probability is crucial because it provides insight into the likelihood of mutants appearing in a population of cells.
For scientists and researchers, knowing this probability allows more informed estimates and predictions about the number of cells needed to find at least one mutant.Key points to remember:
  • Probability of a mutation is calculated as a ratio: mutants per single cell.
  • Higher mutation rates indicate a higher likelihood of mutation in the population.
  • The likelihood of finding a mutant can influence how many samples need to be screened.
Lactose Nonutilizing Mutants
Lactose nonutilizing mutants are those cells that have undergone a specific mutation making them unable to utilize lactose as a food source.
Lactose is a sugar found in milk, and many bacteria can use it as their primary energy source, provided they possess the necessary genetic setup.
In the study of genetics and microbiology, identifying such mutants can be significantly important. These mutants help researchers understand genetic pathways and regulation, as well as generate knowledge about mutations that lead bacteria to lose the ability to metabolize certain substances. In practice:
  • Lactose nonutilizing mutants can reveal information on gene function.
  • They serve as a model to understand similar processes in more complex organisms.
  • These types of experiments contribute to developing treatments by understanding mutations related to antibiotic resistance.
Researchers aim to detect these mutants in large populations, using high mutation rates to ensure the presence of mutants within the samples screened.
Biostatistics in Biology
Biostatistics applies statistical methods to biological problems.
It's the backbone of analyzing genetic research data and is crucial in calculating mutation rates. When we talk about finding mutants in cell populations, biostatistics allows us to use mathematical methods to estimate the number of cells that need to be screened to find at least one mutant.
For example, when a researcher desires a 95% probability of finding a mutant in a cell population, they use statistical formulas to determine the number of cells to be tested. The calculations involve understanding probabilities and using logarithmic functions to solve for the necessary number of trials.
Essential aspects of biostatistics in this context include:
  • Applying probability theories to biological occurrences.
  • Understanding the relationship between sample size and confidence in findings.
  • Using statistical models to make experimental designs more effective.
Biostatistics ensures that biological experiments and the conclusions drawn from them are based on rigorous data interpretation, reducing uncertainty and enhancing the reliability of scientific research.

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Most popular questions from this chapter

Quorum sensing (introduced in Chapter 11 ) allows bacteria to detect the number of neighboring cells and to trigger a response only when this number reaches a critical level. Quorum sensing is used by \(V\). fischeri in light production and by many pathogenic bacteria, including Vibrio cholera, to turn on genes for toxin production only when a critical cell density is reached. Why might quorum sensing be beneficial to pathogenic bacteria?

LuxR is allosterically regulated by the signaling inducer molecule secreted by \(V\). fischeri. What does it mean that LuxR is allosterically regulated?

The bacteria glow in response to a molecule that regulates expression of genes involved in light-producing chemical reactions. The regulator controls production of the genes' mRNA. Therefore, the light-producing genes are under a. transcriptional control. b. translational control. c. post-translational control. d. negative control.

The light-producing genes of \(V\). fischeri are organized in an operon that is under positive control by an activator protein called LuxR. Would you expect the genes of this operon to be transcribed when LuxR is bound or not bound to a DNA regulatory sequence? Explain.

IPTG is a molecule with a structure very similar to lactose. IPTG can be transported into cells by galactoside permease and can bind to the lac repressor protein. However, unlike lactose, IPTG is not broken down by \(\beta\) -galactosidase. Predict what would occur to lac operon regulation if IPTG were added to \(E\). coli growth medium containing no glucose or lactose.

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