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Allelopathic mechanism of pyrogallol to Microcystis aeruginosa PCC7806 (Cyanobacteria): from views of gene expression and antioxidant system.
Chemosphere. 2009 May; 75(7):924-8.C

Abstract

Pyrogallol is a potent allelochemical on Microcystis aeruginosa, but its allelopathic mechanism is not fully known. In order to explore this mechanism, gene expressions for prx, mcyB, psbA, recA, grpE, fabZ under pyrogallol stress were studied, and activities of the main antioxidant enzymes were also measured. The results showed that expression of grpE and recA showed no significant change under pyrogallol stress, while psbA and mcyB were up-regulated at 4 mg L(-1). Both prx and fabZ were up-regulated even under exposure to 1 mg L(-1) pyrogallol concentration. The activities of superoxide dismutase (SOD) and catalase (CAT) were enhanced under pyrogallol stress. Levels of malodialdehyde (MDA) at 2 and 4 mg L(-1) pyrogallol were significantly higher than those of the controls. It was concluded that oxidant damage is an important mechanism for the allelopathic effect of pyrogallol on M. aeruginosa.

Authors+Show Affiliations

Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, PR China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

19201447

Citation

Shao, Jihai, et al. "Allelopathic Mechanism of Pyrogallol to Microcystis Aeruginosa PCC7806 (Cyanobacteria): From Views of Gene Expression and Antioxidant System." Chemosphere, vol. 75, no. 7, 2009, pp. 924-8.
Shao J, Wu Z, Yu G, et al. Allelopathic mechanism of pyrogallol to Microcystis aeruginosa PCC7806 (Cyanobacteria): from views of gene expression and antioxidant system. Chemosphere. 2009;75(7):924-8.
Shao, J., Wu, Z., Yu, G., Peng, X., & Li, R. (2009). Allelopathic mechanism of pyrogallol to Microcystis aeruginosa PCC7806 (Cyanobacteria): from views of gene expression and antioxidant system. Chemosphere, 75(7), 924-8. https://doi.org/10.1016/j.chemosphere.2009.01.021
Shao J, et al. Allelopathic Mechanism of Pyrogallol to Microcystis Aeruginosa PCC7806 (Cyanobacteria): From Views of Gene Expression and Antioxidant System. Chemosphere. 2009;75(7):924-8. PubMed PMID: 19201447.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Allelopathic mechanism of pyrogallol to Microcystis aeruginosa PCC7806 (Cyanobacteria): from views of gene expression and antioxidant system. AU - Shao,Jihai, AU - Wu,Zhongxing, AU - Yu,Gongliang, AU - Peng,Xin, AU - Li,Renhui, Y1 - 2009/02/08/ PY - 2008/10/15/received PY - 2008/12/12/revised PY - 2009/01/02/accepted PY - 2009/2/10/entrez PY - 2009/2/10/pubmed PY - 2009/6/12/medline SP - 924 EP - 8 JF - Chemosphere JO - Chemosphere VL - 75 IS - 7 N2 - Pyrogallol is a potent allelochemical on Microcystis aeruginosa, but its allelopathic mechanism is not fully known. In order to explore this mechanism, gene expressions for prx, mcyB, psbA, recA, grpE, fabZ under pyrogallol stress were studied, and activities of the main antioxidant enzymes were also measured. The results showed that expression of grpE and recA showed no significant change under pyrogallol stress, while psbA and mcyB were up-regulated at 4 mg L(-1). Both prx and fabZ were up-regulated even under exposure to 1 mg L(-1) pyrogallol concentration. The activities of superoxide dismutase (SOD) and catalase (CAT) were enhanced under pyrogallol stress. Levels of malodialdehyde (MDA) at 2 and 4 mg L(-1) pyrogallol were significantly higher than those of the controls. It was concluded that oxidant damage is an important mechanism for the allelopathic effect of pyrogallol on M. aeruginosa. SN - 1879-1298 UR - https://www.unboundmedicine.com/medline/citation/19201447/Allelopathic_mechanism_of_pyrogallol_to_Microcystis_aeruginosa_PCC7806__Cyanobacteria_:_from_views_of_gene_expression_and_antioxidant_system_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0045-6535(09)00037-X DB - PRIME DP - Unbound Medicine ER -