Moukha S M, Wösten H A, Mylius E J, Asther M, Wessels J G
Laboratoire de Biotechnologie des Champignons Filamenteux, Faculté des Sciences de Luminy, Parc Scientifique et Technologique, Marseille, France.
J Bacteriol. 1993 Jun;175(11):3672-8. doi: 10.1128/jb.175.11.3672-3678.1993.
Accumulation of peroxidases and their mRNAs was localized in colonies of Phanerochaete chrysosporium sandwiched between perforated polycarbonate membranes. Northern (RNA) blot analyses of colonial rings and in situ hybridizations with specific probes for manganese(II)-dependent peroxidase (MnP-1) and lignin peroxidase (LiP H8) mRNAs indicated that the expression of MnP-1 and Lip H8 genes started simultaneously in the central area of 3-day-old colonies. With time the signals for both transcripts spread to more-peripheral areas while decreasing in intensity. Furthermore, the appearance of MnP protein, as detected with specific immune serum, immediately followed accumulation of the MnP-1 mRNA transcript. However, LiP protein could be detected only some time after accumulation of LiP H8 mRNA.
过氧化物酶及其mRNA的积累定位于夹在多孔聚碳酸酯膜之间的黄孢原毛平革菌菌落中。对菌落环进行的Northern(RNA)印迹分析以及用锰(II)依赖性过氧化物酶(MnP-1)和木质素过氧化物酶(LiP H8)mRNA的特异性探针进行的原位杂交表明,MnP-1和Lip H8基因的表达在3日龄菌落的中心区域同时开始。随着时间的推移,两种转录本的信号扩散到更外围的区域,同时强度降低。此外,用特异性免疫血清检测到的MnP蛋白的出现紧接着MnP-1 mRNA转录本的积累。然而,LiP蛋白只能在LiP H8 mRNA积累后的一段时间才能检测到。