DETECTION OF CRYII GENE FROM BACILLUS THURINGIENSIS USING POLYMERASE CHAIN REACTION (PCR)

UPT. PERPUSTAKAAN Universitas Esa Unggul Kampus Emas UEU - Jakarta Barat
Phone	:	021-5674223, ext 282
Fax	:
E-mail	:	[email protected]
Website	:	http://library.esaunggul.ac.id
Support (Customer Service) :
[email protected]

Welcome..guys!

Have a problem with your access?
Please, contact our technical support below:

LIVE SUPPORT

Astrid Chrisafi

! ATTENTION !

To facilitate the activation process, please fill out the member application form correctly and completely

Registration activation of our members will process up to max 24 hours (confirm by email). Please wait patiently

Still Confuse?
Please read our User Guide

UEU » Scientific Articles » Bioteknologi
Posted by [email protected] at 11/11/2021 13:06:52 • 434 Views

DETECTION OF CRYII GENE FROM BACILLUS THURINGIENSIS USING POLYMERASE CHAIN REACTION (PCR)

Created by :
F D Wahyuni ( 0323029101 )
Seprianto; H Saraswati

Subject:	BAKTERI MIKROBIOLOGI SERANGGA
Alt. Subject :	BACTERIA MICROBIOLOGY INSECT
Keyword:	Bacillus thuringiensis cryII gene Polymerase Chain Reaction (PCR)

Description:

Bacillus thuringiensis is one species of bacteria that has been applied as a microbiological control agent for pests and a vector of plant disease. The availability of Cry proteins in B. thuringiensis can be acted as a specific insect exterminator that only toxic to certain insects. The cryII gene is an example of a type of cry gene that encodes a CryII Protein. The CryII protein is toxic to Lepidoptera insects which can attack Helicoverpa armigera species which is a corn borer. Polymerase Chain Reaction (PCR) is a general method that can be used to amplify the gene. This research purposed to design a good primer candidate for cryII gene amplification from B. thuringiensis. In silico analysis for designing cryII primer was carried out using some software, such as BLAST for searching cryII gene sequence, Bioedit for sequences alignment, and DINAmelt for analyzing dimer structure of primers. Ten primer candidates were successfully obtained based on the result of the primer3 software. A pair of primer was selected to amplify the cryII gene, with forward primer 5�-GGTAGTGGACCACAGCAGAC- 3�and reverse primer 5�-TCTTCTGGCGCCAAATGGAT-3�. This primer has fulfilled good primer characteristics because it does not cause dimer structure and the resulting amplicons do not form secondary structures. Amplification of the cryI gene by PCR method using selected primer resulting in a PCR product with a length of approximately 800 bp.

Date Create	:	11/11/2021
Type	:	Text
Format	:	pdf
Language	:	Indonesian
Identifier	:	UEU-Article-5_0813
Collection ID	:	5_0813

Source :
IOP Conf. Series: Earth and Environmental Science 743 (2021) 012093

Relation Collection:
Fakultas Ilmu-Ilmu Kesehatan

Coverage :
Civitas Akademika Universitas Esa Unggul

Rights :
@2021 Perpustakaan Universitas Esa Unggul

Publication URL :
https://digilib.esaunggul.ac.id/detection-of-cryii-gene-from-bacillus-thuringiensis-using-polymerase-chain-reaction-pcr-22460.html

[ Free Download - Free for All ]