Carsolio C, Gutiérrez A, Jiménez B, Van Montagu M, Herrera-Estrella A
Centro de Investigación y Estudios Avanzados, Unidad Irapuato, Guanajuato, México.
Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):10903-7. doi: 10.1073/pnas.91.23.10903.
A gene (ech-42; previously named ThEn-42) coding for one of the endochitinases produced by the biocontrol agent Trichoderma harzianum IMI206040 was cloned and characterized. Expression of the cDNA clone in Escherichia coli resulted in bacteria with chitinase activity. This chitinase has been shown to have lytic activity on Botrytis cinerea cell walls in vitro. The ech-42 gene was assigned to a double chromosomal band (chromosome V or VI) upon electrophoretic separation and Southern analysis of the chromosomes. Primer extension analysis indicated that transcription of the gene begins preferentially 109 bp upstream of the translation initiation codon. Expression of ech-42 was strongly enhanced during direct interaction of the mycoparasite with a phytopathogenic fungus when confronted in vitro and by growing it in minimal medium containing chitin as sole carbon source. Similarly, light-induced sporulation resulted in high levels of transcript, suggesting developmental regulation of the gene. The implications of these findings are discussed.
对生物防治剂哈茨木霉IMI206040产生的一种内切几丁质酶编码的基因(ech - 42;以前称为ThEn - 42)进行了克隆和表征。该cDNA克隆在大肠杆菌中的表达产生了具有几丁质酶活性的细菌。已证明这种几丁质酶在体外对灰葡萄孢菌细胞壁具有裂解活性。经染色体的电泳分离和Southern分析,ech - 42基因定位于一条双染色体带(V或VI号染色体)。引物延伸分析表明,该基因的转录优先在翻译起始密码子上游109 bp处开始。当在体外对峙培养并在以几丁质作为唯一碳源的基本培养基中培养时,在这种真菌寄生物与植物病原真菌直接相互作用期间,ech - 42的表达强烈增强。同样,光诱导产孢导致该基因的转录水平很高,表明该基因受发育调控。讨论了这些发现的意义。