Chlamydomonas reinhardtii-expressed multimer of ToAMP4 inhibits the growth of bacteria of both Gram-positive and Gram-negative. (April 2020)
- Record Type:
- Journal Article
- Title:
- Chlamydomonas reinhardtii-expressed multimer of ToAMP4 inhibits the growth of bacteria of both Gram-positive and Gram-negative. (April 2020)
- Main Title:
- Chlamydomonas reinhardtii-expressed multimer of ToAMP4 inhibits the growth of bacteria of both Gram-positive and Gram-negative
- Authors:
- Xue, Bin
Dong, Chun-Ming
Hu, He-He
Dong, Bin
Fan, Zhen-Chuan - Abstract:
- Graphical abstract: Highlights: The recombinant ToAMP4 was expressed in Chlamydomonas reinhardtii for the first time. The expression of recombinant ToAMP4 was stable. The recombinant ToAMP4 had a broad antibacterial spectrum. The recombinant ToAMP4 had good stability, low hemolysis activity and low cytotoxicity. The recombinant ToAMP4 disrupted bacterial cell morphology and membrane integrity. Abstract: The antimicrobial peptide ToAMP4 was isolated from Taraxacum officinale Wigg. flowers. Bacterial-expressed ToAMP4 showed antifungal activity but was inactive against bacteria. In this study, Chlamydomonas reinhardtii was used to express a C-terminal hemagglutinin (HA) and 6×His double tagged three repeats of ToAMP4 (3×ToAMP4)and the 3×ToAMP4-expressing cells were screened to express 3×ToAMP4 stably following continuous passaging for six months. Finally, a yield of 0.32 % of total soluble protein was achieved for 3×ToAMP4, which inhibits the growth of bacteria of both Gram-positive and Gram-negative at a minimum inhibitory concentration between 40 and 50 μg/ml. C. reinhardtii -derived 3×ToAMP4 maintained high stability in a wide range of temperature and pHs, tolerated to protease digestion at different extents and showed low hemolytic activity and cytotoxicity. Moreover, C. reinhardtii -expressed 3×ToAMP4 effectively caused damage on the membrane of targeted bacterial cells. In conclusion, our data show that C. reinhardtii has the potential to be used as a platform for theGraphical abstract: Highlights: The recombinant ToAMP4 was expressed in Chlamydomonas reinhardtii for the first time. The expression of recombinant ToAMP4 was stable. The recombinant ToAMP4 had a broad antibacterial spectrum. The recombinant ToAMP4 had good stability, low hemolysis activity and low cytotoxicity. The recombinant ToAMP4 disrupted bacterial cell morphology and membrane integrity. Abstract: The antimicrobial peptide ToAMP4 was isolated from Taraxacum officinale Wigg. flowers. Bacterial-expressed ToAMP4 showed antifungal activity but was inactive against bacteria. In this study, Chlamydomonas reinhardtii was used to express a C-terminal hemagglutinin (HA) and 6×His double tagged three repeats of ToAMP4 (3×ToAMP4)and the 3×ToAMP4-expressing cells were screened to express 3×ToAMP4 stably following continuous passaging for six months. Finally, a yield of 0.32 % of total soluble protein was achieved for 3×ToAMP4, which inhibits the growth of bacteria of both Gram-positive and Gram-negative at a minimum inhibitory concentration between 40 and 50 μg/ml. C. reinhardtii -derived 3×ToAMP4 maintained high stability in a wide range of temperature and pHs, tolerated to protease digestion at different extents and showed low hemolytic activity and cytotoxicity. Moreover, C. reinhardtii -expressed 3×ToAMP4 effectively caused damage on the membrane of targeted bacterial cells. In conclusion, our data show that C. reinhardtii has the potential to be used as a platform for the production of bioactive ToAMP4. … (more)
- Is Part Of:
- Process biochemistry. Volume 91(2020)
- Journal:
- Process biochemistry
- Issue:
- Volume 91(2020)
- Issue Display:
- Volume 91, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 91
- Issue:
- 2020
- Issue Sort Value:
- 2020-0091-2020-0000
- Page Start:
- 311
- Page End:
- 318
- Publication Date:
- 2020-04
- Subjects:
- Antimicrobial peptide -- ToAMP4 -- Chlamydomonas reinhardtii -- Antibacterial activity
Biochemical engineering -- Periodicals
Biotechnology -- Periodicals
Biochemistry -- periodicals
Biotechnology -- periodicals
Chemical Engineering -- periodicals
Génie biochimique -- Périodiques
Biotechnologie -- Périodiques
Biochemical engineering
Biotechnology
Periodicals
660.63 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13595113 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.procbio.2020.01.001 ↗
- Languages:
- English
- ISSNs:
- 1359-5113
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6849.983500
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- 13492.xml