Cargando…

Characterization of manganese superoxide dismutase from a marine cyanobacterium Leptolyngbya valderiana BDU20041

BACKGROUND: Cyanobacteria are recognized as the primordial organisms to grace the earth with molecular oxygen ~3.5 billion years ago as a result of their oxygenic photosynthesis. This laid a selection pressure for the evolution of antioxidative defense mechanisms to alleviate the toxic effect of act...

Descripción completa

Detalles Bibliográficos
Autores principales: Priya, Balakrishnan, Sivaprasanth, Reddi K, Jensi, Vincent Dhivya, Uma, Lakshmanan, Subramanian, Gopalakrishnan, Prabaharan, Dharmar
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2893185/
https://www.ncbi.nlm.nih.gov/pubmed/20525290
http://dx.doi.org/10.1186/1746-1448-6-6
_version_ 1782183019528847360
author Priya, Balakrishnan
Sivaprasanth, Reddi K
Jensi, Vincent Dhivya
Uma, Lakshmanan
Subramanian, Gopalakrishnan
Prabaharan, Dharmar
author_facet Priya, Balakrishnan
Sivaprasanth, Reddi K
Jensi, Vincent Dhivya
Uma, Lakshmanan
Subramanian, Gopalakrishnan
Prabaharan, Dharmar
author_sort Priya, Balakrishnan
collection PubMed
description BACKGROUND: Cyanobacteria are recognized as the primordial organisms to grace the earth with molecular oxygen ~3.5 billion years ago as a result of their oxygenic photosynthesis. This laid a selection pressure for the evolution of antioxidative defense mechanisms to alleviate the toxic effect of active oxygen species (AOS) in cyanobacteria. Superoxide dismutases (SODs) are metalloenzymes that are the first arsenal in defense mechanism against oxidative stress followed by an array of antioxidative system. Unlike other living organisms, cyanobacteria possess multiple isoforms of SOD. Hence, an attempt was made to demonstrate the oxidative stress tolerance ability of marine cyanobacterium, Leptolyngbya valderiana BDU 20041 and to PCR amplify and sequence the SOD gene, the central enzyme for alleviating stress. RESULT: L. valderiana BDU 20041, a filamentous, non-heterocystous marine cyanobacterium showed tolerance to the tested dye (C.I. Acid Black 1) which is evident by increased in biomass (i.e.) chlorophyll a. The other noticeable change was the total ROS production by culture dosed with dye compared to the control cultures. This prolonged incubation showed sustenance, implying that cyanobacteria maintain their antioxidant levels. The third significant feature was a two-fold increase in SOD activity of dye treated L. valderiana BDU20041 suggesting the role of SOD in alleviating oxidative stress via Asada-Halliwell pathway. Hence, the organism was PCR amplified for SOD gene resulting in an amplicon of 550 bp. The sequence analysis illustrated the presence of first three residues involved in motif; active site residues at H4, 58 and D141 along with highly conserved Mn specific residues. The isolated gene shared 63.8% homology with MnSOD of bacteria confirmed it as Mn isoform. This is the hitherto report on SOD gene from marine cyanobacterium, L. valderiana BDU20041 of Indian subcontinent. CONCLUSION: Generation of Reactive Oxygen Species (ROS) coupled with induction of SOD by marine cyanobacterium, L. valderiana BDU20041 was responsible for alleviating stress caused by an azo dye, C. I. Acid Black 1. The partial SOD gene has been sequenced and based on the active site, motif and metal specific residues; it has been identified as Mn metalloform.
format Text
id pubmed-2893185
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-28931852010-06-29 Characterization of manganese superoxide dismutase from a marine cyanobacterium Leptolyngbya valderiana BDU20041 Priya, Balakrishnan Sivaprasanth, Reddi K Jensi, Vincent Dhivya Uma, Lakshmanan Subramanian, Gopalakrishnan Prabaharan, Dharmar Saline Syst Short Report BACKGROUND: Cyanobacteria are recognized as the primordial organisms to grace the earth with molecular oxygen ~3.5 billion years ago as a result of their oxygenic photosynthesis. This laid a selection pressure for the evolution of antioxidative defense mechanisms to alleviate the toxic effect of active oxygen species (AOS) in cyanobacteria. Superoxide dismutases (SODs) are metalloenzymes that are the first arsenal in defense mechanism against oxidative stress followed by an array of antioxidative system. Unlike other living organisms, cyanobacteria possess multiple isoforms of SOD. Hence, an attempt was made to demonstrate the oxidative stress tolerance ability of marine cyanobacterium, Leptolyngbya valderiana BDU 20041 and to PCR amplify and sequence the SOD gene, the central enzyme for alleviating stress. RESULT: L. valderiana BDU 20041, a filamentous, non-heterocystous marine cyanobacterium showed tolerance to the tested dye (C.I. Acid Black 1) which is evident by increased in biomass (i.e.) chlorophyll a. The other noticeable change was the total ROS production by culture dosed with dye compared to the control cultures. This prolonged incubation showed sustenance, implying that cyanobacteria maintain their antioxidant levels. The third significant feature was a two-fold increase in SOD activity of dye treated L. valderiana BDU20041 suggesting the role of SOD in alleviating oxidative stress via Asada-Halliwell pathway. Hence, the organism was PCR amplified for SOD gene resulting in an amplicon of 550 bp. The sequence analysis illustrated the presence of first three residues involved in motif; active site residues at H4, 58 and D141 along with highly conserved Mn specific residues. The isolated gene shared 63.8% homology with MnSOD of bacteria confirmed it as Mn isoform. This is the hitherto report on SOD gene from marine cyanobacterium, L. valderiana BDU20041 of Indian subcontinent. CONCLUSION: Generation of Reactive Oxygen Species (ROS) coupled with induction of SOD by marine cyanobacterium, L. valderiana BDU20041 was responsible for alleviating stress caused by an azo dye, C. I. Acid Black 1. The partial SOD gene has been sequenced and based on the active site, motif and metal specific residues; it has been identified as Mn metalloform. BioMed Central 2010-06-03 /pmc/articles/PMC2893185/ /pubmed/20525290 http://dx.doi.org/10.1186/1746-1448-6-6 Text en Copyright © 2010 Priya et al; licensee BioMed Central Ltd. https://creativecommons.org/licenses/by/2.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0 (https://creativecommons.org/licenses/by/2.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Priya, Balakrishnan
Sivaprasanth, Reddi K
Jensi, Vincent Dhivya
Uma, Lakshmanan
Subramanian, Gopalakrishnan
Prabaharan, Dharmar
Characterization of manganese superoxide dismutase from a marine cyanobacterium Leptolyngbya valderiana BDU20041
title Characterization of manganese superoxide dismutase from a marine cyanobacterium Leptolyngbya valderiana BDU20041
title_full Characterization of manganese superoxide dismutase from a marine cyanobacterium Leptolyngbya valderiana BDU20041
title_fullStr Characterization of manganese superoxide dismutase from a marine cyanobacterium Leptolyngbya valderiana BDU20041
title_full_unstemmed Characterization of manganese superoxide dismutase from a marine cyanobacterium Leptolyngbya valderiana BDU20041
title_short Characterization of manganese superoxide dismutase from a marine cyanobacterium Leptolyngbya valderiana BDU20041
title_sort characterization of manganese superoxide dismutase from a marine cyanobacterium leptolyngbya valderiana bdu20041
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2893185/
https://www.ncbi.nlm.nih.gov/pubmed/20525290
http://dx.doi.org/10.1186/1746-1448-6-6
work_keys_str_mv AT priyabalakrishnan characterizationofmanganesesuperoxidedismutasefromamarinecyanobacteriumleptolyngbyavalderianabdu20041
AT sivaprasanthreddik characterizationofmanganesesuperoxidedismutasefromamarinecyanobacteriumleptolyngbyavalderianabdu20041
AT jensivincentdhivya characterizationofmanganesesuperoxidedismutasefromamarinecyanobacteriumleptolyngbyavalderianabdu20041
AT umalakshmanan characterizationofmanganesesuperoxidedismutasefromamarinecyanobacteriumleptolyngbyavalderianabdu20041
AT subramaniangopalakrishnan characterizationofmanganesesuperoxidedismutasefromamarinecyanobacteriumleptolyngbyavalderianabdu20041
AT prabaharandharmar characterizationofmanganesesuperoxidedismutasefromamarinecyanobacteriumleptolyngbyavalderianabdu20041