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本文引用的文献

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Determination of serum proteins by means of the biuret reaction.通过双缩脲反应测定血清蛋白。
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Escherichia coli spotted double-strand DNA microarrays: RNA extraction, labeling, hybridization, quality control, and data management.大肠杆菌斑点双链DNA微阵列:RNA提取、标记、杂交、质量控制和数据管理。
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DNA microarray analyses of the long-term adaptive response of Escherichia coli to acetate and propionate.大肠杆菌对乙酸盐和丙酸盐长期适应性反应的DNA微阵列分析。
Appl Environ Microbiol. 2003 Mar;69(3):1759-74. doi: 10.1128/AEM.69.3.1759-1774.2003.
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A polyphosphate kinase (PPK2) widely conserved in bacteria.一种在细菌中广泛保守的多聚磷酸激酶(PPK2)。
Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16678-83. doi: 10.1073/pnas.262655199. Epub 2002 Dec 16.
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Transcriptional analysis of the pst operon of Escherichia coli.大肠杆菌pst操纵子的转录分析
Mol Genet Genomics. 2002 Dec;268(4):518-24. doi: 10.1007/s00438-002-0764-4. Epub 2002 Oct 29.
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LrhA as a new transcriptional key regulator of flagella, motility and chemotaxis genes in Escherichia coli.LrhA作为大肠杆菌中鞭毛、运动性和趋化性基因的一种新的转录关键调节因子。
Mol Microbiol. 2002 Jul;45(2):521-32. doi: 10.1046/j.1365-2958.2002.03032.x.
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Regulatory interactions between the Pho and sigma(B)-dependent general stress regulons of Bacillus subtilis.枯草芽孢杆菌 Pho 和 σ(B) 依赖性一般应激调节子之间的调控相互作用。
Microbiology (Reading). 2002 May;148(Pt 5):1593-1602. doi: 10.1099/00221287-148-5-1593.
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Crystallographic and biochemical analyses of the metal-free Haemophilus influenzae Fe3+-binding protein.无金属的流感嗜血杆菌铁离子结合蛋白的晶体学与生化分析
Biochemistry. 2001 Dec 25;40(51):15631-7. doi: 10.1021/bi0156759.
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Genome-wide analysis of the general stress response in Bacillus subtilis.枯草芽孢杆菌一般应激反应的全基因组分析。
Mol Microbiol. 2001 Aug;41(4):757-74. doi: 10.1046/j.1365-2958.2001.02534.x.
10
Activation by gene amplification of pitB, encoding a third phosphate transporter of Escherichia coli K-12.通过基因扩增激活pitB,pitB编码大肠杆菌K-12的第三种磷酸转运蛋白。
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通过DNA微阵列分析确定的谷氨酸棒杆菌的磷酸盐饥饿刺激因子。

The phosphate starvation stimulon of Corynebacterium glutamicum determined by DNA microarray analyses.

作者信息

Ishige Takeru, Krause Malgorzata, Bott Michael, Wendisch Volker F, Sahm Hermann

机构信息

Institut für Biotechnologie 1, Forschungszentrum Jülich, D-52425 Jülich, Germany.

出版信息

J Bacteriol. 2003 Aug;185(15):4519-29. doi: 10.1128/JB.185.15.4519-4529.2003.

DOI:10.1128/JB.185.15.4519-4529.2003
PMID:12867461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC165763/
Abstract

The phosphate (P(i)) starvation stimulon of Corynebacterium glutamicum was characterized by global gene expression analysis by using DNA microarrays. Hierarchical cluster analysis of the genes showing altered expression 10 to 180 min after a shift from P(i)-sufficient to P(i)-limiting conditions led to identification of five groups comprising 92 genes. Four of these groups included genes which are not directly involved in P metabolism and changed expression presumably due to the reduced growth rate observed after the shift or to the exchange of medium. One group, however, comprised 25 genes, most of which are obviously related to phosphorus (P) uptake and metabolism and exhibited 4- to >30-fold-greater expression after the shift to P(i) limitation. Among these genes, the RNA levels of the pstSCAB (ABC-type P(i) uptake system), glpQ (glycerophosphoryldiester phosphodiesterase), ugpAEBC (ABC-type sn-glycerol 3-phosphate uptake system), phoH (unknown function), nucH (extracellular nuclease), and Cgl0328 (5'-nucleotidase or related esterase) genes were increased, and pstSCAB exhibited a faster response than the other genes. Transcriptional fusion analyses revealed that elevated expression of pstSCAB and ugpAEBC was primarily due to transcriptional regulation. Several genes also involved in P uptake and metabolism were not affected by P(i) starvation; these included the genes encoding a PitA-like P(i) uptake system and a putative Na(+)-dependent P(i) transporter and the genes involved in the metabolism of pyrophosphate and polyphosphate. In summary, a global, time-resolved picture of the response of C. glutamicum to P(i) starvation was obtained.

摘要

通过使用DNA微阵列进行全局基因表达分析,对谷氨酸棒杆菌的磷酸盐(P(i))饥饿刺激子进行了表征。对从P(i)充足条件转变为P(i)限制条件后10至180分钟表达发生变化的基因进行层次聚类分析,鉴定出由92个基因组成的五组。其中四组包括与磷代谢不直接相关的基因,其表达变化可能是由于转变后观察到的生长速率降低或培养基的更换。然而,有一组包含25个基因,其中大多数显然与磷(P)的摄取和代谢有关,并且在转变为P(i)限制后表达增加了4至>30倍。在这些基因中,pstSCAB(ABC型P(i)摄取系统)、glpQ(甘油磷酸二酯磷酸二酯酶)、ugpAEBC(ABC型sn-甘油3-磷酸摄取系统)、phoH(功能未知)、nucH(细胞外核酸酶)和Cgl0328(5'-核苷酸酶或相关酯酶)基因的RNA水平升高,并且pstSCAB比其他基因表现出更快的反应。转录融合分析表明,pstSCAB和ugpAEBC的表达升高主要是由于转录调控。几个也参与磷摄取和代谢的基因不受P(i)饥饿的影响;这些基因包括编码类PitA的P(i)摄取系统和推定的Na(+)依赖性P(i)转运蛋白的基因以及参与焦磷酸和多聚磷酸代谢的基因。总之,获得了谷氨酸棒杆菌对P(i)饥饿反应的全局、时间分辨图谱。