Loading…
Alga-lytic activity of Pseudomonas fluorescens against the red tide causing marine alga Heterosigma akashiwo (Raphidophyceae)
A bacterial strain, HAK-13, exhibited strongest activity against Heterosigma akashiwo and was capable of controlling this bloom forming phytoplankton. Based on 16S rDNA sequences and biochemical and morphological characteristics, the strain HAK-13 was determined to be Pseudomonas fluorescens on the...
Saved in:
Published in: | Biological control 2007-06, Vol.41 (3), p.296-303 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | A bacterial strain, HAK-13, exhibited strongest activity against
Heterosigma akashiwo and was capable of controlling this bloom forming phytoplankton. Based on 16S rDNA sequences and biochemical and morphological characteristics, the strain HAK-13 was determined to be
Pseudomonas fluorescens on the basis of 99.9% similarity with reference strains in the DNA databases. The growth of
H.
akashiwo was strongly suppressed by HAK-13 in all growth phases, with the strongest alga-lytic activity noted against harmful bloom-forming species in the exponential stage (6–22 days). Host range tests showed that HAK-13 also significantly inhibited the growth of
Alexandrium tamarense and
Cochlodinium polykrikoides but could not destroy
Gymnodinium catenatum.
P. fluorescens HAK-13 indirectly attacked
H.
akashiwo by alga-lytic substances that might be located at the compartment of cytoplasmic membrane of the bacterium at a level of 45.86
units/mg of specific activity. The results indicated that
P.
fluorescens HAK-13 caused cell lysis and death of
H.
akashiwo,
A.
tamarense, and
C.
polykrikoides dramatically and
Prorocentrum dentatum slightly. Therefore,
P.
fluorescens HAK-13 has potential for use as a selective biocontrol of harmful algal blooms. |
---|---|
ISSN: | 1049-9644 1090-2112 |
DOI: | 10.1016/j.biocontrol.2007.02.010 |