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Published on March 21, 2008; 10.1104/pp.106.081497

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Received April 11, 2006
Accepted March 11, 2008

Characterization of Cold-responsive Extracellular Chitinase in Bromegrass Cell Cultures and its Relationship to Antifreeze Activity

Toshihide Nakamura , Masaya Ishikawa *, Hiroko Nakatani , and Aska Oda

Environmental Stress Research Unit, Division of Plant Sciences, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan

* Corresponding author; email: isikawam{at}affrc.go.jp.

A cold-responsive chitinase gene, BiCHT1, was isolated from bromegrass (Bromus inermis Leyss cv. Manchar) suspension cells. BiCHT1 mRNA was detected at low levels in non-stressed bromegrass cells, whereas its accumulation was induced by incubation at 10 and 4 °C as detected by Northern and Western blot analyses. BiCHT1 was highly homologous to rye CHT9 known as an antifreeze protein. BiCHT1 was overexpressed in Escherichia coli (E. coli) and bromegrass cells using genetic transformation procedures. BiCHT1 products expressed in both systems had chitinase activity, but the expressed proteins did not affect the growth of ice crystals in any conditions tested. Besides cold stress, the expression of the BiCHT1 gene was up-regulated by exposure to 35°C, but not by salt or osmotic stress, abscisic acid or ethephon. BiCHT1 mRNA did not accumulate in response to methyl jasmonate and salicylic acid, but was slightly increased by prolonged culture at 25°C and only transiently by chitin. Antifreeze activity detected in the culture medium was induced at 4°C but only slightly at 10°C. It was also induced by ethephon treatment, but not by abscisic acid, chitin or prolonged incubation at 25°C. The results of transgenics and expression analyses suggest that the BiCHT1 product is a major protein with chitinase activity secreted in the medium of cold-treated cells and is unlikely to be responsible for the antifreeze activity detected in the culture medium.






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