Effect of actinomycin D isolated from the cultured broth of marine streptomyces spp. On cell division protein FtsZ

© 2020, Chiang Mai University. All rights reserved. In the course of our investigation on antibacterial substances with FtsZ inhibitory effect, actinomycin D was isolated from the ethyl acetate extract of Streptomyces sp. LT3-17. The compound showed antibacterial activities. The MIC values of actino...

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Main Authors: Phennapa Charoenwiwattanakij, Jaturong Pratuangdejkul, Sumet Chongruchiroj, Khanit Suwanborirux, Chitti Thawai, Jiraporn Chingunpitak, Veena Satitpatipan
Other Authors: Chulalongkorn University
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Published: 2020
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/54492
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spelling th-mahidol.544922020-05-05T13:08:21Z Effect of actinomycin D isolated from the cultured broth of marine streptomyces spp. On cell division protein FtsZ Phennapa Charoenwiwattanakij Jaturong Pratuangdejkul Sumet Chongruchiroj Khanit Suwanborirux Chitti Thawai Jiraporn Chingunpitak Veena Satitpatipan Chulalongkorn University Walailak University King Mongkut's Institute of Technology Ladkrabang Mahidol University Biochemistry, Genetics and Molecular Biology Chemistry Materials Science Mathematics Physics and Astronomy © 2020, Chiang Mai University. All rights reserved. In the course of our investigation on antibacterial substances with FtsZ inhibitory effect, actinomycin D was isolated from the ethyl acetate extract of Streptomyces sp. LT3-17. The compound showed antibacterial activities. The MIC values of actinomycin D against Staphylococcus aureus ATCC 25923, Methicillin-resistant Staphylococcus aureus DMST 20654, Bacillus subtilis ATCC 6633, Escherichia coli ATCC 25922, and Pseudomonas aeruginosa ATCC 27853 were 3.13, 0.39, 0.10, 300.00, and 500.00 µg/mL, respectively. The morphology study of E. coli JW0093 treated with the compound showed inhibitory effect on cell elongation. The inhibition of FtsZ activity by actinomycin D was shown as the inhibition of GTPase activity with IC50 value, 20.06 µM. The polymerization of E. coli FtsZ protein (EcFtsZ) treated with 0.01 µM actinomycin D showed the degree of polymerization ratio was less than 1.0 indicating the inhibitory potential of actinomycin D on FtsZ polymerization. In silico study was performed to predict binding mode of actinomycin D into nucleotide binding pocket of the homology model of EcFtsZ protein. From the results of these experiments, the isolation and elucidation methods of actinomycin D as well as its novel mechanism as FtsZ inhibitors have been discovered. 2020-05-05T05:08:34Z 2020-05-05T05:08:34Z 2020-01-01 Article Chiang Mai Journal of Science. Vol.47, No.3 (2020), 362-377 01252526 2-s2.0-85083709777 https://repository.li.mahidol.ac.th/handle/123456789/54492 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85083709777&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Materials Science
Mathematics
Physics and Astronomy
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Materials Science
Mathematics
Physics and Astronomy
Phennapa Charoenwiwattanakij
Jaturong Pratuangdejkul
Sumet Chongruchiroj
Khanit Suwanborirux
Chitti Thawai
Jiraporn Chingunpitak
Veena Satitpatipan
Effect of actinomycin D isolated from the cultured broth of marine streptomyces spp. On cell division protein FtsZ
description © 2020, Chiang Mai University. All rights reserved. In the course of our investigation on antibacterial substances with FtsZ inhibitory effect, actinomycin D was isolated from the ethyl acetate extract of Streptomyces sp. LT3-17. The compound showed antibacterial activities. The MIC values of actinomycin D against Staphylococcus aureus ATCC 25923, Methicillin-resistant Staphylococcus aureus DMST 20654, Bacillus subtilis ATCC 6633, Escherichia coli ATCC 25922, and Pseudomonas aeruginosa ATCC 27853 were 3.13, 0.39, 0.10, 300.00, and 500.00 µg/mL, respectively. The morphology study of E. coli JW0093 treated with the compound showed inhibitory effect on cell elongation. The inhibition of FtsZ activity by actinomycin D was shown as the inhibition of GTPase activity with IC50 value, 20.06 µM. The polymerization of E. coli FtsZ protein (EcFtsZ) treated with 0.01 µM actinomycin D showed the degree of polymerization ratio was less than 1.0 indicating the inhibitory potential of actinomycin D on FtsZ polymerization. In silico study was performed to predict binding mode of actinomycin D into nucleotide binding pocket of the homology model of EcFtsZ protein. From the results of these experiments, the isolation and elucidation methods of actinomycin D as well as its novel mechanism as FtsZ inhibitors have been discovered.
author2 Chulalongkorn University
author_facet Chulalongkorn University
Phennapa Charoenwiwattanakij
Jaturong Pratuangdejkul
Sumet Chongruchiroj
Khanit Suwanborirux
Chitti Thawai
Jiraporn Chingunpitak
Veena Satitpatipan
format Article
author Phennapa Charoenwiwattanakij
Jaturong Pratuangdejkul
Sumet Chongruchiroj
Khanit Suwanborirux
Chitti Thawai
Jiraporn Chingunpitak
Veena Satitpatipan
author_sort Phennapa Charoenwiwattanakij
title Effect of actinomycin D isolated from the cultured broth of marine streptomyces spp. On cell division protein FtsZ
title_short Effect of actinomycin D isolated from the cultured broth of marine streptomyces spp. On cell division protein FtsZ
title_full Effect of actinomycin D isolated from the cultured broth of marine streptomyces spp. On cell division protein FtsZ
title_fullStr Effect of actinomycin D isolated from the cultured broth of marine streptomyces spp. On cell division protein FtsZ
title_full_unstemmed Effect of actinomycin D isolated from the cultured broth of marine streptomyces spp. On cell division protein FtsZ
title_sort effect of actinomycin d isolated from the cultured broth of marine streptomyces spp. on cell division protein ftsz
publishDate 2020
url https://repository.li.mahidol.ac.th/handle/123456789/54492
_version_ 1763487579539243008