Microbial Physiology Lab, National Institute for Biotechnology and Genetic Engineering (NIBGE), P.O. Box 577, Jhang Road, Faisalabad, Pakistan.
World J Microbiol Biotechnol. 2012 Aug;28(8):2749-58. doi: 10.1007/s11274-012-1086-2. Epub 2012 Jun 20.
An Enterobacter sp. Fs-11 was isolated from sunflower rhizosphere, identified on the basis of 16S rRNA gene sequence analysis (GeneBank accession no. GQ179978) and studied for its root colonization and growth promotion ability in sunflower. Morphologically, it was rod shaped Gram-negative, motile bacterium, producing 4.5 μg mL(-1) indole acetic acid in tryptophan-supplemented medium. It utilized 27 out of 95 substrates in BIOLOG GN2 micro plate system. It was able to convert insoluble tri-calcium phosphate to soluble phosphorus up to 43.5 μg mL(-1) with decrease in pH of the medium up to 4.5 after 10 days incubation at 28 ± 2 °C in the Pikovskaya's broth. High performance liquid chromatography of cell free supernatant showed that Fs-11 produced malic acid and gluconic acid (2.43 and 16.64 μg mL(-1), respectively) in Pikovskaya's broth. Analysis of 900 bp fragment of pyrroloquinoline quinine pqqE gene sequence showed 98 % homology with that of E. cloacae pqqE gene. Confocal laser scanning microscope revealed strong colonization of fluorescently labeled Fs-11 with sunflower roots. Sunflower inoculation with Fs-11 and its rifampicin resistant derivative in sterile sand and natural soil showed that Fs-11 colonized sunflower roots up to 30 days after transplanting in both sterile sand as well as natural soil. Moreover, Fs-11 inoculation resulted in increased plant height, fresh weight, dry weight and total phosphorus contents as compared to un-inoculated plants. The data showed that Enterobacter sp. Fs-11 is an efficient phosphate solubilizing and plant growth promoting rhizobacterium and has great potential to be used as bio-inoculant for sunflower under phosphorus deficient conditions.
从向日葵根际中分离到一株肠杆菌属(Enterobacter sp.)菌株 Fs-11,基于 16S rRNA 基因序列分析(基因库登录号:GQ179978)对其进行鉴定,并研究其在向日葵中的定殖和促生能力。该菌呈杆状、革兰氏阴性、运动性细菌,在含色氨酸的培养基中可产生 4.5μg/mL 的吲哚乙酸。在 BIOLOG GN2 微孔板系统中,它能够利用 95 种基质中的 27 种。在 28±2℃的条件下,在 Pikovskaya 肉汤中培养 10 天后,可将不溶性三钙磷酸盐转化为可溶性磷,最高可达 43.5μg/mL,同时培养基的 pH 值下降至 4.5。细胞上清液的高效液相色谱分析表明,Fs-11 在 Pikovskaya 肉汤中产生了苹果酸和葡萄糖酸(分别为 2.43 和 16.64μg/mL)。对吡咯喹啉醌醌氧化还原酶(pqqE)基因 900bp 片段的分析表明,其与阴沟肠杆菌 pqqE 基因的同源性为 98%。共聚焦激光扫描显微镜显示,Fs-11 荧光标记后可强烈定殖于向日葵根系。在无菌砂和自然土壤中,将 Fs-11 及其利福平抗性衍生物接种到向日葵中,结果表明,在无菌砂和自然土壤中,Fs-11 可在移栽后 30 天内定殖于向日葵根部。此外,与未接种的植株相比,Fs-11 接种可提高植株的株高、鲜重、干重和总磷含量。这些数据表明,肠杆菌属 Fs-11 是一种高效的溶磷和促生根际细菌,具有在缺磷条件下作为向日葵生物接种剂的巨大潜力。