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双态致病真菌中半胱氨酸双加氧酶的酶活性和基因表达在霉菌和酵母形态型中均有体现,且存在显著的菌株差异。

Cysteine Dioxygenase Enzyme Activity and Gene Expression in the Dimorphic Pathogenic Fungus Is in both the Mold and Yeast Morphotypes and Exhibits Substantial Strain Variation.

作者信息

Adams Melissa A, Shearer Glenmore

机构信息

Center for Molecular and Cellular Biosciences, The University of Southern Mississippi, 118 College Dr. #5018, Hattiesburg, MS 39406, USA.

出版信息

J Fungi (Basel). 2020 Feb 13;6(1):24. doi: 10.3390/jof6010024.

Abstract

In the dimorphism (mold/yeast) () literature are reports that yeast (the so-called pathogenic form) uniquely expresses a cysteine dioxygenase (CDO, approx. 10,500 dal) activity which the mold morphotype (the so-called saprophytic soil form) does not express (C.F., Kumar et al., Biochem 22, 762, 1983). This yeast-specific CDO activity is postulated to play a critical role in the mold-to-yeast shift. A number of years ago, our lab isolated the gene encoding the cysteine dioxygenase (, Genbank accession AY804144) and noted significant expression in the mold morphotype of several strains and also determined that the predicted protein would be over double the 10,500 dal reported by Kumar et al. Our report demonstrates (in the class 1 Downs strain, the class 2 G271B strain and two Panamanian strains, 184AS and 186AS) that the gene is expressed in both the mold and yeast morphotypes and both morphotypes show significant CDO activity. Furthermore, we show via a FLAG-tag analysis that the expressed protein is approximately 24.7 ± 2.4 kd, in agreement with the putative protein sequence (determined from cDNA sequence) which yields 23.8 kd and is consistent with most other eukaryotic CDO enzymes. Additionally, we demonstrate that intracellular cysteine levels are actually significantly higher in the mold form of the two Panamanian strains, 184AS and 186AS, equal in both mold and yeast in the class 1 Downs strain and significantly higher in yeast of the more pathogenic class 2 G217B strain.

摘要

在双态性(霉菌/酵母)文献中,有报道称酵母(所谓的致病形态)独特地表达一种半胱氨酸双加氧酶(CDO,约10,500道尔顿)活性,而霉菌形态型(所谓的腐生土壤形态)不表达这种活性(C.F.,Kumar等人,《生物化学》22,762,1983)。这种酵母特异性的CDO活性被认为在霉菌向酵母的转变中起关键作用。几年前,我们实验室分离出了编码半胱氨酸双加氧酶的基因(Genbank登录号AY804144),并注意到在几种菌株的霉菌形态型中有显著表达,还确定预测的蛋白质分子量将是Kumar等人报道的10,500道尔顿的两倍多。我们的报告表明(在1类唐斯菌株、2类G271B菌株以及两个巴拿马菌株184AS和186AS中),该基因在霉菌和酵母形态型中均有表达,且两种形态型都显示出显著的CDO活性。此外,我们通过FLAG标签分析表明,表达的蛋白质约为24.7±2.4kd,这与从cDNA序列确定的推定蛋白质序列一致,该推定蛋白质序列产生23.8kd,并且与大多数其他真核CDO酶一致。此外,我们证明,在两个巴拿马菌株184AS和186AS的霉菌形态中,细胞内半胱氨酸水平实际上显著更高,在1类唐斯菌株的霉菌和酵母形态中半胱氨酸水平相等,而在致病性更强的2类G217B菌株的酵母形态中半胱氨酸水平显著更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6527/7151203/aa533f5e34dc/jof-06-00024-g001.jpg

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