Gaid Mariam M, Sircar Debabrata, Beuerle Till, Mitra Adinpunya, Beerhues Ludger
Institute of Pharmaceutical Biology, Technical University of Braunschweig, Mendelssohnstrasse 1, D-38106 Braunschweig, Germany.
J Plant Physiol. 2009 Sep 1;166(13):1343-9. doi: 10.1016/j.jplph.2009.03.003. Epub 2009 May 1.
Cell cultures of Sorbus aucuparia respond to the addition of chitosan with the accumulation of the biphenyl phytoalexin aucuparin. The carbon skeleton of this inducible defense compound is formed by biphenyl synthase (BIS) from benzoyl-CoA and three molecules of malonyl-CoA. The formation of benzoyl-CoA proceeds via benzaldehyde as an intermediate. Benzaldehyde dehydrogenase (BD), which converts benzaldehyde into benzoic acid, was detected in cell-free extracts from S. aucuparia cell cultures. BD and BIS were induced by chitosan treatment. The preferred substrate for BD was benzaldehyde (K(m)=49 microM). Cinnamaldehyde and various hydroxybenzaldehydes were relatively poor substrates. BD activity was strictly dependent on the presence of NAD(+) as a cofactor (K(m)=67 microM).
花楸细胞培养物在添加壳聚糖后会积累联苯植保素花楸苷。这种诱导性防御化合物的碳骨架由联苯合酶(BIS)从苯甲酰辅酶A和三分子丙二酰辅酶A形成。苯甲酰辅酶A的形成以苯甲醛作为中间体进行。在花楸细胞培养物的无细胞提取物中检测到将苯甲醛转化为苯甲酸的苯甲醛脱氢酶(BD)。壳聚糖处理可诱导BD和BIS。BD的首选底物是苯甲醛(米氏常数K(m)=49微摩尔)。肉桂醛和各种羟基苯甲醛是相对较差的底物。BD活性严格依赖于作为辅因子的NAD⁺的存在(米氏常数K(m)=67微摩尔)。