A cytotoxic pentadecapeptide from a South African Didemnid tunicate

publisher version === The rate of discovery of new natural product chemical entities has plateaued, and unique populations of endemic, biologically diverse sessile marine organisms represent increasingly critical opportunities to discover new chemistry. Discovery of the mandelalides [1] as potent in...

Full description

Bibliographic Details
Main Authors: Gallegos, D, Serrill, J, Parker-Nance, Shirley, Dorrington, Rosemary, Ishmael, J, McPhail, K L
Format: Others
Language:English
Published: Georg Thieme Verlag KG 2016
Online Access:http://hdl.handle.net/10962/65935
https://doi.org/10.1055/s-0036-1596683
id ndltd-netd.ac.za-oai-union.ndltd.org-rhodes-vital-28863
record_format oai_dc
spelling ndltd-netd.ac.za-oai-union.ndltd.org-rhodes-vital-288632018-08-25T05:06:29ZA cytotoxic pentadecapeptide from a South African Didemnid tunicateGallegos, DSerrill, JParker-Nance, ShirleyDorrington, RosemaryIshmael, JMcPhail, K Lpublisher versionThe rate of discovery of new natural product chemical entities has plateaued, and unique populations of endemic, biologically diverse sessile marine organisms represent increasingly critical opportunities to discover new chemistry. Discovery of the mandelalides [1] as potent inhibitors of cancer cell growth from the new South African tunicate Lissoclinum mandelai is an example of the diverse suites of metabolites with potent biological activities that have been isolated from tunicates and other filter-feeding sessile marine organisms that house complex microbial consortia. Further investigation of archived and new tunicate collections from Algoa Bay, South Africa, has revealed a group of didemnid tunicates with an unusual gelatinous morphology similar to Lissoclinum mandelai. Using a bioassay-guided isolation approach, a new “gelatinous” species of the genus Didemnum has yielded a cytotoxic pentadecapeptide with a molecular mass of 1603.7688 Da, comprising fifteen residues including both proteinogenic and non-proteinogenic amino acids. The pure compound inhibited both HeLa cervical cancer and NCI-H460 non-small cell lung cancer cell lines when tested at 30 nM in preliminary assays against cells seeded at low densities. Inhibition of cancer cells at low starting density may be indicative of an anti-proliferative mechanism of action. The compound did not show antibacterial activity against Vibrio cholera. Didemnin B and its clinically approved analogue dehydrodidemnin B (plitidepsin, Aplidin®) [2, 3] are important macrocyclic depsipeptides from a didemnid tunicate. The pentadecapeptide reported here provides justification for our continued investigation of unique, endemic didemnid tunicates from South Africa as a source of new macrocyclic natural products with cytotoxic, anti-viral or antimicrobial activity.We acknowledge the South African government for permission to collect the subject tunicate (Collection Permit No. 278 RES2013/43)Georg Thieme Verlag KG2016textarticlepdfhttp://hdl.handle.net/10962/65935vital:28863https://doi.org/10.1055/s-0036-1596683EnglishPlanta MedicaThieme Planta MedicaUse of this resource is governed by the terms and conditions of the National Library of South Africa Copyright Act (http://www.nlsa.ac.za/downloads/Copyright%20Act.pdf)
collection NDLTD
language English
format Others
sources NDLTD
description publisher version === The rate of discovery of new natural product chemical entities has plateaued, and unique populations of endemic, biologically diverse sessile marine organisms represent increasingly critical opportunities to discover new chemistry. Discovery of the mandelalides [1] as potent inhibitors of cancer cell growth from the new South African tunicate Lissoclinum mandelai is an example of the diverse suites of metabolites with potent biological activities that have been isolated from tunicates and other filter-feeding sessile marine organisms that house complex microbial consortia. Further investigation of archived and new tunicate collections from Algoa Bay, South Africa, has revealed a group of didemnid tunicates with an unusual gelatinous morphology similar to Lissoclinum mandelai. Using a bioassay-guided isolation approach, a new “gelatinous” species of the genus Didemnum has yielded a cytotoxic pentadecapeptide with a molecular mass of 1603.7688 Da, comprising fifteen residues including both proteinogenic and non-proteinogenic amino acids. The pure compound inhibited both HeLa cervical cancer and NCI-H460 non-small cell lung cancer cell lines when tested at 30 nM in preliminary assays against cells seeded at low densities. Inhibition of cancer cells at low starting density may be indicative of an anti-proliferative mechanism of action. The compound did not show antibacterial activity against Vibrio cholera. Didemnin B and its clinically approved analogue dehydrodidemnin B (plitidepsin, Aplidin®) [2, 3] are important macrocyclic depsipeptides from a didemnid tunicate. The pentadecapeptide reported here provides justification for our continued investigation of unique, endemic didemnid tunicates from South Africa as a source of new macrocyclic natural products with cytotoxic, anti-viral or antimicrobial activity. === We acknowledge the South African government for permission to collect the subject tunicate (Collection Permit No. 278 RES2013/43)
author Gallegos, D
Serrill, J
Parker-Nance, Shirley
Dorrington, Rosemary
Ishmael, J
McPhail, K L
spellingShingle Gallegos, D
Serrill, J
Parker-Nance, Shirley
Dorrington, Rosemary
Ishmael, J
McPhail, K L
A cytotoxic pentadecapeptide from a South African Didemnid tunicate
author_facet Gallegos, D
Serrill, J
Parker-Nance, Shirley
Dorrington, Rosemary
Ishmael, J
McPhail, K L
author_sort Gallegos, D
title A cytotoxic pentadecapeptide from a South African Didemnid tunicate
title_short A cytotoxic pentadecapeptide from a South African Didemnid tunicate
title_full A cytotoxic pentadecapeptide from a South African Didemnid tunicate
title_fullStr A cytotoxic pentadecapeptide from a South African Didemnid tunicate
title_full_unstemmed A cytotoxic pentadecapeptide from a South African Didemnid tunicate
title_sort cytotoxic pentadecapeptide from a south african didemnid tunicate
publisher Georg Thieme Verlag KG
publishDate 2016
url http://hdl.handle.net/10962/65935
https://doi.org/10.1055/s-0036-1596683
work_keys_str_mv AT gallegosd acytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT serrillj acytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT parkernanceshirley acytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT dorringtonrosemary acytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT ishmaelj acytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT mcphailkl acytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT gallegosd cytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT serrillj cytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT parkernanceshirley cytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT dorringtonrosemary cytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT ishmaelj cytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
AT mcphailkl cytotoxicpentadecapeptidefromasouthafricandidemnidtunicate
_version_ 1718727054192541696