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Synthesis of xylanolytic enzymes and other carbohydrases by the fungus Penicillium canescens: Transformants with an altered copy number of the gene xlnR and an encoding transcriptional activator
Authors:V. A. Serebryanyi  O. A. Sinitsyna  E. A. Fedorova  O. N. Okunev  O. A. Bekkarevich  L. M. Sokolova  E. A. Vavilova  Yu. P. Vitetsky  A. P. Sinitsyn
Affiliation:(1) State Research Institute of Genetics and Selection of Industrial Microorganisms, Moscow, 113545, Russia;(2) Lomonosov Moscow State University, Moscow, 119899, Russia;(3) Skryabin Institute of Physiology and Biochemistry of Microorganisms, Pushchino, Moscow oblast, 142290, Russia
Abstract:A fragment of Penicillium canescens genomic DNA carrying the xlnR gene coding for a translational activator of xylanolytic genes was isolated. It was demonstrated that a loss of this function in genetically modified transformants resulted in a drastic decrease in the production of P. canescens major xylanases and had a negative effect on the syntheses of several other extracellular xylanases. An increase in the dose of the xlnR gene elevated the xylanolytic activity as well as the activities of a number of other auxiliary enzymes involved in xylan degradation. The activities of two P. canescens major secreted enzymes—β-galactosidase and α-L-arabinofuranosidase—appeared weakly dependent on the translational activator xlnR.
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