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利用竞争性逆转录聚合酶链反应分析皱落假丝酵母中脂肪酶编码基因家族。

Analysis of the gene family encoding lipases in Candida rugosa by competitive reverse transcription-PCR.

作者信息

Lee G C, Tang S J, Sun K H, Shaw J F

机构信息

Institute of Biochemistry, National Yang-Ming University, Taipei, Taiwan 11211.

出版信息

Appl Environ Microbiol. 1999 Sep;65(9):3888-95. doi: 10.1128/AEM.65.9.3888-3895.1999.

Abstract

Synthesis of multiple extracellular lipases in Candida rugosa has been demonstrated. However, it is difficult to characterize the expression spectrum of lip genes, since the sequences of the lip multigene family are very closely related. A competitive reverse transcription-PCR assay was developed to quantify the expression of lip genes. In agreement with the protein profile, the abundance of lip mRNAs was found to be (in decreasing order) lip1, lip3, lip2, lip5, and lip4. To analyze the effects of different culture conditions, the transcript concentrations for these mRNA species were normalized relative to the values for gpd, encoding glyceraldehyde-3-phosphate dehydrogenase. In relative terms, lip1 and lip3 were highly and constitutively expressed (about 10(5) molecules per microg of total RNA) whereas the other inducible lip genes, especially lip4, showed significant changes in mRNA expression under different culture conditions. These results indicate that differential transcriptional control of lip genes results in multiple forms of lipase proteins.

摘要

已经证明皱落假丝酵母中会合成多种细胞外脂肪酶。然而,由于脂肪酶多基因家族的序列非常相似,因此很难确定脂肪酶基因的表达谱。我们开发了一种竞争性逆转录 - PCR 测定法来定量脂肪酶基因的表达。与蛋白质谱一致,发现脂肪酶 mRNA 的丰度(从高到低)为 lip1、lip3、lip2、lip5 和 lip4。为了分析不同培养条件的影响,将这些 mRNA 种类的转录本浓度相对于编码甘油醛 - 3 - 磷酸脱氢酶的 gpd 的值进行归一化。相对而言,lip1 和 lip3 高度且组成性表达(每微克总 RNA 约 10⁵ 个分子),而其他可诱导的脂肪酶基因,特别是 lip4,在不同培养条件下 mRNA 表达显示出显著变化。这些结果表明脂肪酶基因的差异转录控制导致了多种形式的脂肪酶蛋白。

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