Department of Microbiology, Vidyasagar University, Midnapore, West Bengal, India.
J Appl Microbiol. 2013 Jan;114(1):84-95. doi: 10.1111/jam.12030. Epub 2012 Oct 29.
To examine tannic acid (TA) utilization capacity by nitrogen-fixing bacteria, Azotobacter sp. SSB81, and identify the intermediate products during biotransformation. Another aim of this work is to investigate the effects of TA on major biopolymers like extracellular polysaccharide (EPS) and polyhydroxybutyrate (PHB) synthesis.
Tannic acid utilization and tolerance capacity of the strain was determined according to CLSI method. Intermediate products were identified using high-performance liquid chromatography, LC-MS/MS and (1) H NMR analysis. Intermediates were quantified by multiple reactions monitoring using LC-MS/MS. The strain was able to tolerate a high level of TA and utilized through enzymatic system. Growth of Azotobacter in TA-supplemented medium was characterized by an extended lag phase and decreased growth rate. Presence of TA catalytic enzymes as tannase, polyphenol oxidase (PPO) and phenol decarboxylase was confirmed in cell lysate using their specific substrates. PPO activity was more prominent in TA-supplemented mineral medium after 48 h of growth when gallic to ellagic acid (EA) reversible reaction was remarkable. Phase contrast and scanning electron microscopic analysis revealed elongated and irregular size of Azotobacter cells in response to TA. (1) H NMR analysis indicated that TA was transformed into gallic acid (GA), EA and pyrogallol. Biopolymer (EPS and PHB) production was decreased several folds in the presence of TA compared with cells grown in only glucose medium.
This is the first evidence on the biotransformation of TA by Azotobacter and also elevated level of EA production from gallotannins. Azotobacter has developed the mechanism to utilize TA for their carbon and energy source.
The widespread occurrence and exploitation of Azotobacter sp. strain SSB81 in agricultural and forest soil have an additional advantage to utilize the soil-accumulated TA and detoxifies the allelopathic effect of constant accumulated TA in soil.
研究固氮菌 Azotobacter sp. SSB81 对鞣酸(TA)的利用能力,并鉴定生物转化过程中的中间产物。本工作的另一个目的是研究 TA 对胞外多糖(EPS)和聚羟基丁酸(PHB)等主要生物聚合物合成的影响。
根据 CLSI 方法确定菌株对 TA 的利用和耐受能力。使用高效液相色谱、LC-MS/MS 和(1)H NMR 分析鉴定中间产物。使用 LC-MS/MS 进行多重反应监测定量中间产物。该菌株能够耐受高水平的 TA 并通过酶系统进行利用。在添加 TA 的培养基中,固氮菌的生长表现出延长的迟滞期和降低的生长速率。使用其特异性底物在细胞裂解物中证实了 TA 催化酶如鞣酸酶、多酚氧化酶(PPO)和酚脱羧酶的存在。在添加 TA 的矿物培养基中培养 48 小时后,PPO 活性更为明显,此时发生了从没食子酸(GA)到鞣花酸(EA)的可逆反应。相差和扫描电子显微镜分析表明,固氮菌细胞在 TA 存在下呈伸长和不规则形状。(1)H NMR 分析表明 TA 被转化为没食子酸(GA)、EA 和焦儿茶酸。与仅在葡萄糖培养基中生长的细胞相比,生物聚合物(EPS 和 PHB)的产量降低了数倍。
这是首次证明 Azotobacter 对 TA 的生物转化,以及从鞣花单宁中产生更高水平的 EA。固氮菌已经开发出利用 TA 作为其碳和能源来源的机制。
固氮菌 SSB81 在农业和森林土壤中的广泛存在和利用具有额外的优势,可以利用土壤中积累的 TA,并减轻土壤中不断积累的 TA 的化感作用。