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根系衍生底物对荧光假单胞菌HK44中nah-lux基因表达的影响:对根际多环芳烃生物降解的意义。

Effect of root-derived substrates on the expression of nah-lux genes in Pseudomonas fluorescens HK44: implications for PAH biodegradation in the rhizosphere.

作者信息

Kamath Roopa, Schnoor Jerald L, Alvarez Pedro J J

机构信息

Department of Civil and Environmental Engineering, The University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

Environ Sci Technol. 2004 Mar 15;38(6):1740-5. doi: 10.1021/es0306258.

Abstract

The bioluminescent reporter strain Pseudomonas fluorescens HK44 with a nah-lux fusion, was used to investigate the effect of root material (from hybrid poplars, willow, kou, milo, Osage orange, mulberry, and switch grass) and potential root-derived substrates (e.g., sugars, carboxylic acids, amino acids, and phenolics) on the expression of nahG, one of the genes responsible for naphthalene dioxygenase transcription. Whereas nahG was induced by some phenolic substrates that could be released by plants (i.e., salicylate, methyl salicylate, and acetyl salicylate), no induction by root extracts was observed. Rather, increasing root extract concentrations (50 to 275 mg L(-1) as total organic carbon) inhibited nahG expression in assays with cells concurrently exposed to naphthalene. Root extracts also decreased nahG expression at the individual cell level during naphthalene degradation assays. However, treatments with root extracts exhibited significantly higher microbial growth and overall bioluminescence, indicating a higher level of nahG expression by the resulting larger microbial population. This generally resulted in faster naphthalene degradation rates, suggesting that plant-promoted proliferation of competent genotypes could compensate for the interference that labile substrates exert on the expression of genes that code for the degradation of polynuclear aromatic hydrocarbons (PAHs). This could explain the faster PAH degradation commonly reported in planted than in unplanted soils.

摘要

采用带有nah - lux融合基因的生物发光报告菌株荧光假单胞菌HK44,研究根材料(来自杂交杨树、柳树、寇氏豆梨、蜀黍、桑橙、桑树和柳枝稷)以及潜在的根衍生底物(如糖类、羧酸、氨基酸和酚类)对nahG表达的影响,nahG是负责萘双加氧酶转录的基因之一。虽然nahG可被一些植物可能释放的酚类底物(即水杨酸、水杨酸甲酯和乙酰水杨酸)诱导,但未观察到根提取物的诱导作用。相反,在细胞同时暴露于萘的试验中,增加根提取物浓度(以总有机碳计为50至275 mg L(-1))会抑制nahG表达。在萘降解试验中,根提取物在单个细胞水平上也降低了nahG表达。然而,用根提取物处理后微生物生长和总体生物发光显著更高,表明由此产生的更大微生物群体中nahG表达水平更高。这通常导致萘降解速率更快,表明植物促进有能力的基因型增殖可以补偿不稳定底物对编码多环芳烃(PAH)降解的基因表达的干扰。这可以解释在种植土壤中通常比未种植土壤中PAH降解更快的现象。

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