Mamarabadi Mojtaba, Jensen Birgit, Lübeck Mette
Plant Pathology Section, Department of Plant Biology, Faculty of Life Sciences, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg C, Copenhagen, Denmark.
Curr Genet. 2008 Aug;54(2):57-70. doi: 10.1007/s00294-008-0199-5. Epub 2008 Jun 24.
Three endochitinase-encoding genes, cr-ech58, cr-ech42 and cr-ech37 were identified and characterised from the mycoparasitic C. rosea strain IK726. The endochitinase activity was specifically induced in media containing chitin or Fusarium culmorum cell walls as sole carbon sources. RT-PCR analysis showed that the three genes were differentially expressed. The expression of the cr-ech42 and cr-ech37 genes was triggered by F. culmorum cell walls and chitin whereas glucose repressed their expression. In contrast, the expression of cr-ech58 was not triggered by F. culmorum cell walls and chitin, suggesting a different role for this endochitinase. Phylogenetically, the cr-ech42 and cr-ech37 genes showed to be orthologous to endochitinase 42 and 37 kDa encoding genes from other mycoparasitic fungi, while no orthologous gene for the cr-ech58 gene was found. Three genetically modified mutants of C. rosea were made by disruption of the endochitinase genes via Agrobacterium-mediated transformation and their biocontrol activity was evaluated. While in planta bioassays showed no significant difference in biocontrol efficacy between the disruptants and the wildtype, the real time RT-PCR analysis showed that disruption of each endochitinase gene affected the activity of C. rosea during interaction with F. culmorum in liquid cultures.
从寄生真菌粉红粘帚霉IK726中鉴定并表征了三个编码内切几丁质酶的基因,即cr-ech58、cr-ech42和cr-ech37。内切几丁质酶活性在以几丁质或禾谷镰刀菌细胞壁作为唯一碳源的培养基中被特异性诱导。RT-PCR分析表明这三个基因的表达存在差异。cr-ech42和cr-ech37基因的表达由禾谷镰刀菌细胞壁和几丁质触发,而葡萄糖会抑制它们的表达。相反,cr-ech58的表达不会被禾谷镰刀菌细胞壁和几丁质触发,这表明该内切几丁质酶具有不同的作用。在系统发育上,cr-ech42和cr-ech37基因与其他寄生真菌中编码42 kDa和37 kDa内切几丁质酶的基因是直系同源的,而未发现与cr-ech58基因直系同源的基因。通过农杆菌介导的转化破坏几丁质酶基因,构建了三个粉红粘帚霉的基因修饰突变体,并评估了它们的生物防治活性。虽然植物体内生物测定表明突变体和野生型在生物防治效果上没有显著差异,但实时RT-PCR分析表明,在液体培养中与禾谷镰刀菌相互作用期间,每个几丁质酶基因的破坏都会影响粉红粘帚霉的活性。