Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology

MPT64 is a specific protein that is secreted by Mycobacterium tuberculosis complex (MTBC). The objective of this study was to obtain optimum culture conditions for MPT64 synthetic gene expression in Escherichia coli BL21 (DE3) by response surface methodology (RSM). The RSM was undertaken to optimize...

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Main Authors: Kusuma, Sri Agung Fitri, Parwati, Ida, Rostinawati, Tina, Yusuf, Muhammad, Fadhlillah, Muhammad, Ahyudanari, Risa R., Rukayadi, Yaya, Subroto, Toto
Format: Article
Language:English
Published: Elsevier 2019
Online Access:http://psasir.upm.edu.my/id/eprint/81564/1/Optimization%20of%20culture%20conditions%20for%20Mpt64%20synthetic%20gene%20expression%20in%20Escherichia%20coli%20BL21%20%28DE3%29%20using%20surface%20response%20methodology.pdf
http://psasir.upm.edu.my/id/eprint/81564/
https://www.sciencedirect.com/science/article/pii/S2405844019364011#!
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spelling my.upm.eprints.815642021-01-28T15:53:21Z http://psasir.upm.edu.my/id/eprint/81564/ Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology Kusuma, Sri Agung Fitri Parwati, Ida Rostinawati, Tina Yusuf, Muhammad Fadhlillah, Muhammad Ahyudanari, Risa R. Rukayadi, Yaya Subroto, Toto MPT64 is a specific protein that is secreted by Mycobacterium tuberculosis complex (MTBC). The objective of this study was to obtain optimum culture conditions for MPT64 synthetic gene expression in Escherichia coli BL21 (DE3) by response surface methodology (RSM). The RSM was undertaken to optimize the culture conditions under different cultivation conditions (medium concentration, induction time and inducer concentration), designed by the factorial Box-Bhenken using Minitab 17 statistical software. From the randomized combination, 15 treatments and three center point repetitions were obtained. Furthermore, expression methods were carried out in the flask scale fermentation in accordance with the predetermined design. Then, the MPT64 protein in the cytoplasm of E. coli cell was isolated and characterized using sodium dodecyl sulfate polyacrilamide electrophoresis (SDS-PAGE) then quantified using the ImageJ program. The optimum conditions were two-fold medium concentration (tryptone 20 mg/mL, yeast extract 10 mg/mL, and sodium chloride 20 mg/mL), 5 h of induction time and 4 mM rhamnose. The average concentration of recombinant MPT64 at optimum conditions was 0.0392 mg/mL, higher than the predicted concentration of 0.0311 mg/mL. In conclusion, the relationship between the selected optimization parameters strongly influenced the level of MPT64 gene expression in E. coli BL21 (DE3). Elsevier 2019 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/81564/1/Optimization%20of%20culture%20conditions%20for%20Mpt64%20synthetic%20gene%20expression%20in%20Escherichia%20coli%20BL21%20%28DE3%29%20using%20surface%20response%20methodology.pdf Kusuma, Sri Agung Fitri and Parwati, Ida and Rostinawati, Tina and Yusuf, Muhammad and Fadhlillah, Muhammad and Ahyudanari, Risa R. and Rukayadi, Yaya and Subroto, Toto (2019) Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology. Heliyon, 5 (11). art. no. e02741. pp. 1-9. ISSN 2405-8440 https://www.sciencedirect.com/science/article/pii/S2405844019364011#! 10.1016/j.heliyon.2019.e02741
institution Universiti Putra Malaysia
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language English
description MPT64 is a specific protein that is secreted by Mycobacterium tuberculosis complex (MTBC). The objective of this study was to obtain optimum culture conditions for MPT64 synthetic gene expression in Escherichia coli BL21 (DE3) by response surface methodology (RSM). The RSM was undertaken to optimize the culture conditions under different cultivation conditions (medium concentration, induction time and inducer concentration), designed by the factorial Box-Bhenken using Minitab 17 statistical software. From the randomized combination, 15 treatments and three center point repetitions were obtained. Furthermore, expression methods were carried out in the flask scale fermentation in accordance with the predetermined design. Then, the MPT64 protein in the cytoplasm of E. coli cell was isolated and characterized using sodium dodecyl sulfate polyacrilamide electrophoresis (SDS-PAGE) then quantified using the ImageJ program. The optimum conditions were two-fold medium concentration (tryptone 20 mg/mL, yeast extract 10 mg/mL, and sodium chloride 20 mg/mL), 5 h of induction time and 4 mM rhamnose. The average concentration of recombinant MPT64 at optimum conditions was 0.0392 mg/mL, higher than the predicted concentration of 0.0311 mg/mL. In conclusion, the relationship between the selected optimization parameters strongly influenced the level of MPT64 gene expression in E. coli BL21 (DE3).
format Article
author Kusuma, Sri Agung Fitri
Parwati, Ida
Rostinawati, Tina
Yusuf, Muhammad
Fadhlillah, Muhammad
Ahyudanari, Risa R.
Rukayadi, Yaya
Subroto, Toto
spellingShingle Kusuma, Sri Agung Fitri
Parwati, Ida
Rostinawati, Tina
Yusuf, Muhammad
Fadhlillah, Muhammad
Ahyudanari, Risa R.
Rukayadi, Yaya
Subroto, Toto
Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology
author_facet Kusuma, Sri Agung Fitri
Parwati, Ida
Rostinawati, Tina
Yusuf, Muhammad
Fadhlillah, Muhammad
Ahyudanari, Risa R.
Rukayadi, Yaya
Subroto, Toto
author_sort Kusuma, Sri Agung Fitri
title Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology
title_short Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology
title_full Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology
title_fullStr Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology
title_full_unstemmed Optimization of culture conditions for Mpt64 synthetic gene expression in Escherichia coli BL21 (DE3) using surface response methodology
title_sort optimization of culture conditions for mpt64 synthetic gene expression in escherichia coli bl21 (de3) using surface response methodology
publisher Elsevier
publishDate 2019
url http://psasir.upm.edu.my/id/eprint/81564/1/Optimization%20of%20culture%20conditions%20for%20Mpt64%20synthetic%20gene%20expression%20in%20Escherichia%20coli%20BL21%20%28DE3%29%20using%20surface%20response%20methodology.pdf
http://psasir.upm.edu.my/id/eprint/81564/
https://www.sciencedirect.com/science/article/pii/S2405844019364011#!
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