Hottes Alison K, Meewan Maliwan, Yang Desiree, Arana Naomi, Romero Pedro, McAdams Harley H, Stephens Craig
Departments of Electrical Engineering. Developmental Biology, Stanford University, Stanford, California 94305, USA.
J Bacteriol. 2004 Mar;186(5):1448-61. doi: 10.1128/JB.186.5.1448-1461.2004.
Microarray analysis was used to examine gene expression in the freshwater oligotrophic bacterium Caulobacter crescentus during growth on three standard laboratory media, including peptone-yeast extract medium (PYE) and minimal salts medium with glucose or xylose as the carbon source. Nearly 400 genes (approximately 10% of the genome) varied significantly in expression between at least two of these media. The differentially expressed genes included many encoding transport systems, most notably diverse TonB-dependent outer membrane channels of unknown substrate specificity. Amino acid degradation pathways constituted the largest class of genes induced in PYE. In contrast, many of the genes upregulated in minimal media encoded enzymes for synthesis of amino acids, including incorporation of ammonia and sulfate into glutamate and cysteine. Glucose availability induced expression of genes encoding enzymes of the Entner-Doudoroff pathway, which was demonstrated here through mutational analysis to be essential in C. crescentus for growth on glucose. Xylose induced expression of genes encoding several hydrolytic exoenzymes as well as an operon that may encode a novel pathway for xylose catabolism. A conserved DNA motif upstream of many xylose-induced genes was identified and shown to confer xylose-specific expression. Xylose is an abundant component of xylan in plant cell walls, and the microarray data suggest that in addition to serving as a carbon source for growth of C. crescentus, this pentose may be interpreted as a signal to produce enzymes associated with plant polymer degradation.
利用微阵列分析来检测淡水贫营养细菌新月柄杆菌在三种标准实验室培养基上生长期间的基因表达,这三种培养基包括蛋白胨 - 酵母提取物培养基(PYE)以及以葡萄糖或木糖作为碳源的基本盐培养基。在这些培养基中,至少有两种之间近400个基因(约占基因组的10%)的表达存在显著差异。差异表达的基因包括许多编码转运系统的基因,最显著的是多种底物特异性未知的依赖TonB的外膜通道。氨基酸降解途径构成了在PYE中诱导表达的最大一类基因。相比之下,在基本培养基中上调的许多基因编码用于氨基酸合成的酶,包括将氨和硫酸盐掺入谷氨酸和半胱氨酸。葡萄糖的可利用性诱导了编码Entner - Doudoroff途径酶的基因的表达,通过突变分析证明该途径在新月柄杆菌利用葡萄糖生长过程中至关重要。木糖诱导了编码几种水解性外切酶的基因以及一个可能编码木糖分解代谢新途径的操纵子的表达。在许多木糖诱导基因上游鉴定出一个保守的DNA基序,并表明其赋予木糖特异性表达。木糖是植物细胞壁中木聚糖的丰富成分,微阵列数据表明,除了作为新月柄杆菌生长的碳源外,这种戊糖可能被解读为一种信号,促使产生与植物聚合物降解相关的酶。