NO-degradation by alfalfa class 1 hemoglobin (Mhb 1):: a possible link to PR-1a gene expression in Mhb1-overproducing tobacco plants

被引:53
作者
Seregélyes, C
Igamberdiev, AU
Maassen, A
Hennig, J
Dudits, D
Hill, RD [1 ]
机构
[1] Univ Manitoba, Dept Plant Sci, Winnipeg, MB R3T 2N2, Canada
[2] Polish Acad Sci, Inst Biochem & Biophys CEMB, PL-02106 Warsaw, Poland
[3] Hungarian Acad Sci, Biol Res Ctr, Inst Plant Biol, H-6701 Szeged, Hungary
基金
加拿大自然科学与工程研究理事会;
关键词
class1; hemoglobin; nitric oxide; purification; hexacoordinate; pathogen; PR-1a;
D O I
10.1016/j.febslet.2004.06.055
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tobacco plants overproducing alfalfa class 1 hemoglobin (HOT plants) have been shown to have reduced necrotic symptom development. Here, we show that this altered pathogenic response is linked to a significant increase in the nitric oxide (NO)-affected pathogenesis-related (PR-1a) transcript accumulation in the transgenic plants. Homogenates of HOT transgenic seedlings were also found to have higher NO-scavenging activity than non-transformed ones. The NO-scavenging properties of recombinant alfalfa class1 hemoglobin have been examined. Recombinant Mhb1 (rMhb1) was produced in bacteria and purified using polvethylene glycol (10-25%) fractionation, chromatography on DEAE-Sephacel, and Phenyl Superose columns. After the final purification step, the obtained preparations were near homogeneous and had a molecular weight of 44 kDa determined by size-exclusion chromatography and 23 kDa by SDS-PAGE, indicating that rMhb1 is a dimer. The protein participated in NO-degradation activity with NAD(P)H as a cofactor. After ion-exchange columns, addition of FAD was necessary for exhibiting maximal NO-degradation activity. The NAD(P)H-dependent NO-scavenging activity of rMhb1, which is similar to that of barley hemoglobin, supports a conclusion that both monocot and dicot class 1 hemoglobins can affect cellular NO levels by scavenging NO formed during hypoxia, pathogen attack and other stresses. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 66
页数:6
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