Zeilinger S, Galhaup C, Payer K, Woo S L, Mach R L, Fekete C, Lorito M, Kubicek C P
Abteilung für Mikrobielle Biochemie, Institut für Biochemische Technologie und Mikrobiologie, TU Wien, Getreidemarkt 9, Wien, A-1060, Austria.
Fungal Genet Biol. 1999 Mar;26(2):131-40. doi: 10.1006/fgbi.1998.1111.
For monitoring chitinase expression during mycoparasitism of Trichoderma harzianum in situ, we constructed strains containing fusions of green fluorescent protein (GFP) to the 5'-regulatory sequences of the T. harzianum nag1 (N-acetyl-beta-d-glucosaminidase-encoding) and ech42 (42-kDa endochitinase-encoding) genes. Confronting these strains with Rhizoctonia solani led to induction of gene expression before (ech42) or after (nag1) physical contact. A 12-kDa cut-off membrane separating the two fungi abolished ech42 expression, indicating that macromolecules are involved in its precontact activation. No ech42 expression was triggered by culture filtrates of R. solani or by placing T. harzianum onto plates previously colonized by R. solani. Instead, high expression occurred upon incubation of T. harzianum with the supernatant of R. solani cell walls digested with culture filtrates or purified endochitinase 42 (CHIT42, encoded by ech42) from T. harzianum. The chitinase inhibitor allosamidin blocked ech42 expression and reduced inhibition of R. solani growth during confrontation. The results indicate that ech42 is expressed before contact of T. harzianum with R. solani and its induction is triggered by soluble chitooligosaccharides produced by constitutive activity of CHIT42 and/or other chitinolytic enzymes.
为了原位监测哈茨木霉在菌寄生过程中的几丁质酶表达,我们构建了含有绿色荧光蛋白(GFP)与哈茨木霉nag1(编码N - 乙酰 - β - D - 氨基葡萄糖苷酶)和ech42(编码42 kDa内切几丁质酶)基因5'调控序列融合体的菌株。将这些菌株与立枯丝核菌对峙培养,导致在物理接触之前(ech42)或之后(nag1)基因表达被诱导。一层12 kDa截留分子量的膜将两种真菌隔开,消除了ech42的表达,表明大分子参与了其接触前的激活过程。立枯丝核菌的培养滤液或把哈茨木霉放置在先前被立枯丝核菌定殖的平板上均未触发ech42的表达。相反,当哈茨木霉与用培养滤液消化的立枯丝核菌细胞壁上清液或哈茨木霉纯化的内切几丁质酶42(由ech42编码的CHIT42)一起孵育时,会出现高表达。几丁质酶抑制剂别洛沙米定阻断了ech42的表达,并在对峙培养期间降低了对立枯丝核菌生长的抑制作用。结果表明,ech42在哈茨木霉与立枯丝核菌接触之前就已表达,其诱导是由CHIT42和/或其他几丁质分解酶的组成型活性产生的可溶性壳寡糖触发的。