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Ch. 9 - Biotechnology & DNA Technology
Tortora - Microbiology: An Introduction 14th Edition
Tortora14th EditionMicrobiology: An IntroductionISBN: 9780138200398당신이 사용하는 게 아니라요?교과서 변경
9장, 문제 3

Which of the following is the fourth basic step to genetically modify a cell?
a. Transformation
b. Ligation
c. Plasmid cleavage
d. Restriction-enzyme digestion of gene
e. Isolation of gene

검증된 단계별 안내
1
Understand the general sequence of steps involved in genetically modifying a cell. Typically, the process includes: (1) isolation of the gene of interest, (2) restriction-enzyme digestion of the gene, (3) plasmid cleavage, (4) ligation, and (5) transformation.
Step 1: Isolation of the gene involves extracting the specific DNA segment that you want to insert into the host cell.
Step 2: Restriction-enzyme digestion of the gene means cutting the isolated gene at specific sequences using restriction enzymes to create compatible ends for insertion.
Step 3: Plasmid cleavage refers to cutting the plasmid vector with the same restriction enzymes to open it up for the insertion of the gene.
Step 4: Ligation is the process of joining the gene fragment and the plasmid vector together using the enzyme DNA ligase, forming a recombinant DNA molecule ready for introduction into the host cell.

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주요 개념

질문에 올바르게 답하기 위해 반드시 이해해야 하는 핵심 개념들은 다음과 같습니다.

Steps in Genetic Modification

Genetic modification involves a series of steps to alter an organism's DNA. These typically include isolating the gene of interest, cutting DNA with restriction enzymes, ligating the gene into a vector, and introducing the recombinant DNA into a host cell via transformation.
추천 영상:

Restriction Enzymes and DNA Cleavage

Restriction enzymes are proteins that cut DNA at specific sequences, enabling precise excision of genes. This step is crucial for preparing both the gene of interest and the plasmid vector for ligation, ensuring compatible ends for joining.
추천 영상:
가이드 코스
03:27
1a) Use Restriction Enzymes

Transformation in Genetic Engineering

Transformation is the process of introducing recombinant DNA into a host cell, often bacteria, allowing the cell to express the new gene. It is typically the final step after constructing the recombinant plasmid, enabling propagation and study of the modified gene.
추천 영상:
가이드 코스
03:06
Bacterial Transformation