de Vries Ronald P, Jansen Jenny, Aguilar Guillermo, Parenicová Lucie, Joosten Vivi, Wülfert Florian, Benen Jacques A E, Visser Jaap
Molecular Genetics of Industrial Microorganisms, Wageningen University, The Netherlands.
FEBS Lett. 2002 Oct 23;530(1-3):41-7. doi: 10.1016/s0014-5793(02)03391-4.
The expression of 26 pectinolytic genes from Aspergillus niger was studied in a wild type strain and a CreA derepressed strain, under 16 different growth conditions, to obtain an expression profile for each gene. These expression profiles were then submitted to cluster analysis to identify subsets of genes with similar expression profiles. With the exception of the feruloyl esterase encoding genes, all genes were expressed in the presence of D-galacturonic acid, polygalacturonate, and/or sugar beet pectin. Despite this general observation five distinct groups of genes were identified. The major group consisted of 12 genes of which the corresponding enzymes act on the pectin backbone and for which the expression, in general, is higher after 8 and 24 h of incubation, than after 2 or 4 h. Two other groups of genes encoding pectin main chain acting enzymes were detected. Two additional groups contained genes encoding L-arabinose and D-galactose releasing enzymes, and ferulic acid releasing enzymes, respectively. The genes encoding beta-galactosidase and the L-arabinose releasing enzymes were not only expressed in the presence of D-galacturonic acid, but also in the presence of L-arabinose, suggesting that they are under the control of two regulatory systems. Similarly, the rhamnogalacturonan acetylesterase encoding gene was not only expressed in the presence of D-galacturonic acid, polygalacturonate and sugar beet pectin, but also in the presence of L-rhamnose. The data presented provides indications for a general pectinolytic regulatory system responding to D-galacturonic acid or a metabolite derived from it. In addition, subsets of pectinolytic genes are expressed in response to the presence of L-arabinose, L-rhamnose or ferulic acid.
在野生型菌株和 CreA 去阻遏菌株中,于 16 种不同生长条件下研究了黑曲霉 26 个果胶分解酶基因的表达情况,以获得每个基因的表达谱。然后将这些表达谱进行聚类分析,以鉴定具有相似表达谱的基因子集。除了编码阿魏酸酯酶的基因外,所有基因在 D-半乳糖醛酸、聚半乳糖醛酸和/或甜菜果胶存在的情况下均有表达。尽管有这一普遍观察结果,但仍鉴定出了五组不同的基因。主要的一组由 12 个基因组成,其相应的酶作用于果胶主链,总体而言,在培养 8 小时和 24 小时后的表达高于培养 2 小时或 4 小时后的表达。还检测到另外两组编码作用于果胶主链的酶的基因。另外两组分别包含编码释放 L-阿拉伯糖和 D-半乳糖的酶以及释放阿魏酸的酶的基因。编码β-半乳糖苷酶和释放 L-阿拉伯糖的酶的基因不仅在 D-半乳糖醛酸存在时表达,而且在 L-阿拉伯糖存在时也表达,这表明它们受两种调节系统的控制。同样,编码鼠李糖半乳糖醛酸乙酰酯酶的基因不仅在 D-半乳糖醛酸、聚半乳糖醛酸和甜菜果胶存在时表达,而且在 L-鼠李糖存在时也表达。所呈现的数据为响应 D-半乳糖醛酸或其衍生代谢物的一般果胶分解调节系统提供了线索。此外,果胶分解酶基因的子集在 L-阿拉伯糖、L-鼠李糖或阿魏酸存在时表达。