This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kamei, I.
Right arrow Articles by Kondo, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kamei, I.
Right arrow Articles by Kondo, R.
Agricola
Right arrow Articles by Kamei, I.
Right arrow Articles by Kondo, R.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, May 2008, p. 2709-2716, Vol. 74, No. 9
0099-2240/08/$08.00+0     doi:10.1128/AEM.02257-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Saline-Dependent Regulation of Manganese Peroxidase Genes in the Hypersaline-Tolerant White Rot Fungus Phlebia sp. Strain MG-60{triangledown}

Ichiro Kamei, Chieko Daikoku, Yuji Tsutsumi,* and Ryuichiro Kondo

Department of Forest and Forest Products Sciences, Faculty of Agriculture, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan

Received 3 October 2007/ Accepted 15 February 2008

The expression pattern of manganese peroxidases (MnPs) in nitrogen-limited cultures of the saline-tolerant fungus Phlebia sp. strain MG-60 is differentially regulated under hypersaline conditions at the mRNA level. When MG-60 was cultured in nitrogen-limited medium (LNM) containing 3% (wt/vol) sea salts (LN-SSM), higher activity of MnPs was observed than that observed in normal medium (LNM). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis demonstrated that two MnP isoenzymes were de novo synthesized in the culture of LN-SSM. Three MnP-encoding genes (MGmnp1, MGmnp2, and MGmnp3) were isolated by reverse transcription (RT)-PCR and rapid amplification of cDNA ends PCR techniques. The corresponding isozymes were identified by peptide mass fingerprinting analysis. MnP isozymes encoded by MGmnp2 and MGmnp3 were observed mainly in LN-SSM. Real-time RT-PCR analysis revealed high levels of MGmnp2 and MGmnp3 transcripts in LN-SSM 48 h after the addition of 2% NaCl. The induction of MnP production and the accumulation of gene transcripts by saline were well correlated in the presence of Mn2+. However, in the absence of Mn2+, there was no clear correlation between mnp transcripts levels and MnP activity, suggesting posttranscriptional regulation by Mn2+.


* Corresponding author. Mailing address: Department of Forest and Forest Products Sciences, Faculty of Agriculture, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan. Phone: 81-092-642-4282. Fax: 81-092-642-4282. E-mail: y-tsutsu{at}agr.kyushu-u.ac.jp

{triangledown} Published ahead of print on 29 February 2008.


Applied and Environmental Microbiology, May 2008, p. 2709-2716, Vol. 74, No. 9
0099-2240/08/$08.00+0     doi:10.1128/AEM.02257-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.