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在模拟溶解氧梯度条件下,对根瘤农杆菌 ATCC 31749 中负责支链淀粉生物合成的基因进行序列和转录分析。

Sequence and transcriptional analysis of the genes responsible for curdlan biosynthesis in Agrobacterium sp. ATCC 31749 under simulated dissolved oxygen gradients conditions.

机构信息

Key Laboratory of Industrial Biotechnology of Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi, China.

出版信息

Appl Microbiol Biotechnol. 2011 Jul;91(1):163-75. doi: 10.1007/s00253-011-3243-1. Epub 2011 Apr 7.

DOI:10.1007/s00253-011-3243-1
PMID:21472535
Abstract

Expression at the mRNA level of ten selected genes in Agrobacterium sp. ATCC 31749 under various dissolved oxygen (DO) levels during curdlan fermentation related to electron transfer chain (ETC), tricarboxylic acid (TCA) cycle, peptidoglycan/lipopolysaccharide biosynthesis, and uridine diphosphate (UDP)-glucose biosynthesis were determined by qRT-PCR. Experiments were performed at DO levels of 30%, 50%, and 75%, as well as under low-oxygen conditions. The effect of high cell density on transcriptional response of the above genes under low oxygen was also studied. Besides cytochrome d (cyd A), the transcription levels of all the other genes were increased at higher DO and reached maximum at 50% DO. Under 75% DO, the transcriptional levels of all the genes were repressed. In addition, transcription levels of icd, sdh, cyo A, and fix N genes did not exhibit significant fluctuation with high cell density culture under low oxygen. These results suggested a mechanism for DO regulation of curdlan synthesis through regulation of transcriptional levels of ETCs, TCA, and UDP-glucose synthesis genes during curdlan fermentation. To our knowledge, this is the first report that DO concentration apparently regulates curdlan biosynthesis in Agrobacterium sp. ATCC 31749 providing essential lead for the optimization of the fermentation at the industrial scale.

摘要

通过 qRT-PCR 测定了与电子传递链 (ETC)、三羧酸 (TCA) 循环、肽聚糖/脂多糖生物合成和尿苷二磷酸 (UDP)-葡萄糖生物合成相关的各种溶解氧 (DO) 水平下农杆菌 sp.ATCC31749 中 10 个选定基因在凝溶胶发酵中的 mRNA 水平表达。实验在 DO 水平为 30%、50%和 75%以及低氧条件下进行。还研究了高细胞密度对低氧下上述基因转录响应的影响。除细胞色素 d (cydA) 外,所有其他基因的转录水平在较高 DO 下增加,并在 50% DO 时达到最大值。在 75% DO 下,所有基因的转录水平均受到抑制。此外,在低氧下高细胞密度培养时,icd、sdh、cyoA 和 fixN 基因的转录水平没有明显波动。这些结果表明,在凝溶胶发酵过程中,通过调节 ETC、TCA 和 UDP-葡萄糖合成基因的转录水平,DO 调节凝溶胶合成的机制。据我们所知,这是首次报道 DO 浓度明显调节农杆菌 sp.ATCC31749 中凝溶胶生物合成的报道,为在工业规模上优化发酵提供了必要的依据。

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