Effect of toxin gene promoter on expression of chloramphenicol acetyltransferase gene (cat) in Bacillus thuringiensis
2
Issued Date
2024
Copyright Date
1992
Resource Type
Language
eng
File Type
application/pdf
No. of Pages/File Size
xv, 159 leaves : ill.
Access Rights
open access
Rights
ผลงานนี้เป็นลิขสิทธิ์ของมหาวิทยาลัยมหิดล ขอสงวนไว้สำหรับเพื่อการศึกษาเท่านั้น ต้องอ้างอิงแหล่งที่มา ห้ามดัดแปลงเนื้อหา และห้ามนำไปใช้เพื่อการค้า
Rights Holder(s)
Mahidol University
Bibliographic Citation
Thesis (M.Sc. (Microbiology))--Mahidol University, 1992
Suggested Citation
Supat Chareonpornwattana Effect of toxin gene promoter on expression of chloramphenicol acetyltransferase gene (cat) in Bacillus thuringiensis. Thesis (M.Sc. (Microbiology))--Mahidol University, 1992. Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/99808
Title
Effect of toxin gene promoter on expression of chloramphenicol acetyltransferase gene (cat) in Bacillus thuringiensis
Alternative Title(s)
ผลของ promoter จาก toxin gene ต่อการแสดงออกของยืน chloramphenicol acetyltransferase (cat) ใน Bacillus thuringiensis
Author(s)
Abstract
A BamH I-PstI fragment harbouring the promoter region of cry IV gene encoding 130 kDa Bacillus thuringiensis subsp. israelensis mosquitocidal toxin protein from pBTC1 was cloned into the promoter probe plasmid vector, pPL703. The recombinant plasmid pPLC1 was transformed into Bacilus megaterium strain 0-016 by protoplast transformation and subsequently was transferred from the transformant to Bacillus thuringiensis subsp. israelensis strain o4Q2-72 and 4Q2-72 by conjugation-like process with the frequency of 2.1 x 10-7 and 1.7 x 10-7 respectively (number of transconjugant Per number of recipient before mating). The presence of cloned promoter region in the constructed plasmid was confirmed by restriction pattern and Southern blot hybridization. The expression level of chloramphenicol acetyltransferase gene (cat) was determined by measuring the specific activity of the enzyme chloramphenical acetyltransferase (CAT). The cat gene product was assayed in crude extracts obtained from lysozyme treated B.megaterium strain 0-016 transformants and Bacillus thuringiensis subsp. israelensis transconjugants. Both transformant and transconjugants were grown in NBS medium (nutrient broth supplemented with minerals) and harvested at the various growth phases, namely, mid exponential, To, T2 and T8. It was shown that the inserted promoter region from cry IV gene conferred the post exponential promoter activity according to the growth pattern when compared to those harbouring the relevant plasmid, pPL603, pPL703 and pTF6. There was no significant difference in term of plasmid copy number in all these plasmids in Bacillus thuringiensis host. Finally, the recombinant plasmid was stably maintained in Bacillus megaterium strain 0-016 transformant, but highly stable in Bacillus thuringiensis subsp. israelensis c4Q2-72 and 4Q2-72 transconjugant upon daily subculture for at least 4 weeks in LB broth medium without any selective pressure.
Description
Microbiology (Mahidol University 1992)
Degree Name
Master of Science
Degree Level
Master's degree
Degree Department
Faculty of Science
Degree Discipline
Microbiology
Degree Grantor(s)
Mahidol University