Vanden Wymelenberg A, Cullen D, Spear R, Andrews J
USDA, Forest Service, Forest Products Laboratory, Madison, WI 53705, USA.
FEMS Microbiol Lett. 1999 Dec 15;181(2):205-9. doi: 10.1111/j.1574-6968.1999.tb08845.x.
A mutant form of the jellyfish cDNA encoding green fluorescent protein (GFP) was fused to the promoter of the Aureobasidium pullulans xylanase gene xynA and the expression vector pxynEGFP was introduced into A. pullulans. In a manner consistent with regulation of the native xynA gene, gfp activity was induced by xylose and repressed by glucose. The marker may be useful for monitoring populations of A. pullulans in situ and for identifying transcriptional control elements of xynA.
将编码绿色荧光蛋白(GFP)的水母cDNA突变形式与出芽短梗霉木聚糖酶基因xynA的启动子融合,并将表达载体pxynEGFP导入出芽短梗霉。与天然xynA基因的调控方式一致,gfp活性由木糖诱导并被葡萄糖抑制。该标记物可能有助于原位监测出芽短梗霉的群体,并用于鉴定xynA的转录控制元件。