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耐冷克雷伯氏菌 NACASA1 对单宁酸的降解及其产物的植物毒性评估。

Degradation of tannic acid by cold-adapted Klebsiella sp NACASA1 and phytotoxicity assessment of tannic acid and its degradation products.

机构信息

Department of Power Mechanical Engineering, National Tsing Hua University, No. 101 Sec. 2 Kuang Fu Road, Hsinchu, Taiwan, Republic of China.

出版信息

Environ Sci Pollut Res Int. 2011 Aug;18(7):1129-38. doi: 10.1007/s11356-011-0468-6. Epub 2011 Feb 19.

Abstract

BACKGROUND, AIM, AND SCOPE: The focus of the present study is to know the potential of bacterial isolate for tannic acid degradation at low temperature. Also, we tried to evaluate the suitability of phytotoxicity testing protocol for the determination of tannic acid toxicity.

METHODS

Screening for tannic acid degrading bacterial strains was carried out by using microbial isolation techniques. The 16S rDNA amplicon of the isolate was used to identify the isolate. The effect of different concentrations of tannic acid and its degradation products on germination of Vigna unguiculata was evaluated. The study was carried out to determine total sugar and starch content of the used seeds and even to check the presence of α-amylase activity during seed germination.

RESULTS

The isolated bacterium was identified as Klebsiella sp NACASA1 and it showed degradation of tannic acid in 40 (±0.85***) h at 15°C and pH 7.0. A gradual decrease in root/shoot length was observed with increasing concentration of tannic acid. There was 95.11 (±0.24**)% inhibition in α-amylase activity at 20,000 ppm tannic acid, as compared to control. No such effects were observed on germination, root-shoot length, and α-amylase activity with tannic acid degradation products.

CONCLUSIONS

The results obtained confirmed that tannic acid may act as a toxic agent in plant cells. The simple biodegradation process presented in this study was found to be effective in reducing toxicity of tannic acid. Also, it reveals the potential of soil bacterium to degrade tannic acid at low temperature.

摘要

背景、目的和范围:本研究的重点是了解细菌分离株在低温下降解单宁酸的潜力。此外,我们还试图评估植物毒性测试方案用于确定单宁酸毒性的适用性。

方法

采用微生物分离技术对单宁酸降解细菌菌株进行筛选。使用分离株的 16S rDNA 扩增子鉴定分离株。评估不同浓度的单宁酸及其降解产物对豇豆发芽的影响。进行这项研究是为了确定所用种子的总糖和淀粉含量,甚至检查种子发芽过程中α-淀粉酶活性的存在。

结果

分离出的细菌被鉴定为克氏杆菌 NACASA1,它在 15°C 和 pH 7.0 下 40(±0.85***)小时内显示出单宁酸的降解。随着单宁酸浓度的增加,根/苗长逐渐下降。与对照相比,在 20000ppm 单宁酸时,α-淀粉酶活性抑制了 95.11(±0.24**)%。单宁酸降解产物对发芽、根/苗长和α-淀粉酶活性没有这种影响。

结论

所得结果证实,单宁酸可能在植物细胞中充当有毒物质。本研究中提出的简单生物降解过程被发现可有效降低单宁酸的毒性。此外,它还揭示了土壤细菌在低温下降解单宁酸的潜力。

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