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Bacterial Transformation Reteach

Bacterial Transformation Reteach

Assessment

Presentation

Science

9th - 12th Grade

Practice Problem

Medium

NGSS
HS-LS1-1, HS-LS3-2, MS-LS2-1

+1

Standards-aligned

Created by

Erynn Hayes

Used 1+ times

FREE Resource

26 Slides • 23 Questions

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Multiple Choice

How do the structural components of bacteria, such as the cell wall and nucleoid DNA, contribute to their ability to undergo transformation?

1
The cell wall prevents DNA uptake, and the nucleoid DNA degrades foreign genes.
2

The cell wall allows DNA uptake, and the nucleoid DNA facilitates genetic integration using plasmids.

3
The cell wall restricts DNA absorption, and the nucleoid DNA impedes genetic exchange.
4
The cell membrane blocks DNA entry, while plasmid DNA hinders integration.

4

Multiple Choice

Why is bacterial transformation considered a significant process in genetic engineering?

1

It allows bacteria to reproduce faster

2

It enables the introduction of new genes into bacteria

3

It increases bacterial resistance to antibiotics

4

It helps bacteria survive in extreme environments

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Multiple Choice

Which structure in a bacterial cell is responsible for movement?

1

Flagellum

2

Pili

3

Capsule

4

Ribosomes

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Multiple Select

Select all the functions of the bacterial capsule.

1

Protects bacteria from toxic compounds

2

Helps bacteria adhere to surfaces

3

Main source of DNA

4

Makes proteins

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Multiple Choice

Which of the following statements best describes the role of plasmids in bacteria?

1

Plasmids carry genes that often give bacteria a genetic advantage.

2

Plasmids are the main source of DNA in bacteria.

3

Plasmids make proteins for the cell.

4

Plasmids maintain cell shape.

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Open Ended

Explain how plasmids contribute to genetic transformation in bacteria.

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Multiple Choice

Which enzyme is used to cut both plant DNA and plasmid DNA in the process shown?

1

Ligase

2

Restriction enzyme

3

Polymerase

4

Helicase

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Multiple Choice

Explain why it is important for the target gene to be inserted in the correct orientation in a plasmid for bacterial expression.

1
Correct orientation is only necessary for plasmid stability.
2

Inserting the gene in any direction will enhance bacterial growth with the incorrect trait being replicated.

3
It is important for the target gene to be inserted in the correct orientation to ensure proper transcription and translation for effective bacterial expression.
4
The orientation of the target gene does not affect protein synthesis.

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Open Ended

Describe the steps involved in producing recombinant insulin as shown in the diagram.

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Multiple Choice

Which organism is the original source of Green Fluorescent Protein (GFP)?

1

Jellyfish

2

Bacteria

3

Corn

4

Fish

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Multiple Choice

GFP is used to identify ___ organisms.

1
transgenic
2

artificial

3

natural

4

incorporated

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Multiple Choice

Which of the following are applications of GFP as a visual marker?

1

Study of protein synthesis

2

Cell movement

3

Formation of organs

4

All of the above

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Open Ended

Explain how GFP can be used as a visual tracer or marker in biological research.

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Open Ended

What are some examples of genetic engineering in agriculture and medicine?

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Fill in the Blanks

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Multiple Choice

What is the function of the 'ori' region in a plasmid?

1

It allows bacteria to make copies of the plasmid.

2

It codes for a protein.

3

It is used for transcription.

4

It is the site for translation.

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Multiple Select

Which of the following statements about genetic transformation are correct?

1

Genetic transformation occurs when a cell takes up DNA and expresses the genes on that DNA.

2

Only bacteria can be genetically transformed.

3

Genetic transformation cannot occur in plants.

4

Many types of cells, including human cells, can be transformed.

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Fill in the Blanks

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Open Ended

Explain how a gene cloned into a plasmid can lead to protein production in bacteria.

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Multiple Choice

Which is the correct sequence for the process of genetic transformation?

1

bacterial cells transferred to cold CaCl2 , plasma with foreign DNA added bacteria , cells heat shocked at 42oC , cells spread on agar petri dish , bacteria given time to grow on petri dish

2

bacterial cells transferred to cold CaCl2 , cells heat shocked at 42oC , plasma with foreign DNA added bacteria , bacteria given time to grow on petri dish , cells spread on agar petri dish

3

plasma with foreign DNA added bacteria , bacterial cells transferred to cold CaCl2 , cells spread on agar petri dish , bacteria given time to grow on petri dish , cells heat shocked at 42oC

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