体外再生Tinospora cordifolia (Willd.) Hook.f. & Thomson--一种具有多用途治疗意义的植物的精英化学型选择、抗病原活性、次生代谢物指纹图谱分析

IF 2.3 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Avijit Chakraborty, Suproteem Mukherjee, Diptesh Biswas, Indranil Santra, Tarun Halder, Md Mabud Alam, Kumaresh Bera, Biswajit Ghosh
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引用次数: 0

摘要

Tinospora cordifolia(Willd.)尿路感染(UTI)病原体对多种药物具有耐药性(MDR),是当今人们日益关注的死亡率和抗菌药耐药性问题,本研究的重点是通过植物化合物定量和抗菌活性检测筛选出一种精英植物化学型。我们从西孟加拉邦不同的农业气候区收集了 12 种这种植物,并通过溶剂优化进行了粗提取。样品 TC 07 在甲醇中的粗萃取率最高。所有 12 种样品提取物对 8 种病原体都有抗菌效果,产生了显著的抑菌区,其中 TC 07 对金黄色葡萄球菌的最大抑菌区为 16.37 ± 0.12 mm。通过高效薄层色谱法对提取物进行评估,结果表明 TC 07 中的小檗碱(5.05 ± 0.05 mg/g)和巴马汀(3.00 ± 0.11 mg/g)含量最高,明显高于其他品种。因此,通过比较这些数据,TC 07 被认为是精英化学型,并被引入离体培养进行保存。在含有 2.0 毫克/升 6-苄基氨基嘌呤和 1.0 毫克/升 meta-Topolin 的 MS 培养基中,获得了最多的芽数(16.39 ± 0.09)。在体外条件下对植物进行了适应性培养,并通过高效液相色谱法确认了生物活性化合物的最佳产量。通过染色体数目测定和起始密码子定向多态性(SCoT),确保了再生植株的细胞遗传稳定性。因此,本研究为小檗碱和巴马汀的优化生产和控制 MDR-UTI 病原体提供了一种简单、有效且可重复的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Elite chemotype selection, antipathogenic activities, secondary metabolite fingerprinting of in vitro regenerated Tinospora cordifolia (Willd.) Hook.f. & Thomson – a plant with multipurpose therapeutic significance

Elite chemotype selection, antipathogenic activities, secondary metabolite fingerprinting of in vitro regenerated Tinospora cordifolia (Willd.) Hook.f. & Thomson – a plant with multipurpose therapeutic significance

Tinospora cordifolia (Willd.) Hook.f. & Thomson is an ethnomedicinal plant belonging to the family Menispermaceae, known for its multi-disciplinary use. The present study is focused on selecting an elite plant chemotype through phytocompound quantification and antimicrobial activity assay against multi-drug-resistant (MDR) urinary-tract-infecting (UTI) pathogens, being a growing concern for mortality and antimicrobial resistance nowadays. Twelve accessions of this plant were collected from different agro-climatic zones of West Bengal, and crude extraction was done by solvent optimization. Sample TC 07 resulted in maximum crude extract yield in methanol. All twelve sample extracts showed antimicrobial efficacy against eight pathogens producing significant inhibition zones, while TC 07 resulting maximum inhibition zone of 16.37 ± 0.12 mm against Staphylococcus aureus. Extracts were evaluated through high-performance thin-layer chromatography, which resulted in optimum amount of berberine (5.05 ± 0.05 mg/g) and palmatine (3.00 ± 0.11 mg/g) in TC 07, significantly higher compared to other accessions. Therefore, comparing the data, TC 07 was considered as the elite chemotype and introduced in in vitro culture for conservation. The maximum number of shoot (16.39 ± 0.09) production was obtained in MS medium containing 2.0 mg/l 6-Benzylaminopurine and 1.0 mg/l meta-Topolin. The plant was acclimatized in ex-vitro condition and confirmed for optimum bioactive compound production through high-performance liquid chromatography. The cytogenetic stability of the regenerated plantlets was ensured using chromosome number determination, and through start codon targeted (SCoT) polymorphism. Therefore, this study provides a simple, validated and reproducible method for optimal berberine and palmatine production and controlling MDR-UTI pathogens.

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来源期刊
Plant Cell, Tissue and Organ Culture
Plant Cell, Tissue and Organ Culture 生物-生物工程与应用微生物
CiteScore
5.40
自引率
13.30%
发文量
203
审稿时长
3.3 months
期刊介绍: This journal highlights the myriad breakthrough technologies and discoveries in plant biology and biotechnology. Plant Cell, Tissue and Organ Culture (PCTOC: Journal of Plant Biotechnology) details high-throughput analysis of gene function and expression, gene silencing and overexpression analyses, RNAi, siRNA, and miRNA studies, and much more. It examines the transcriptional and/or translational events involved in gene regulation as well as those molecular controls involved in morphogenesis of plant cells and tissues. The journal also covers practical and applied plant biotechnology, including regeneration, organogenesis and somatic embryogenesis, gene transfer, gene flow, secondary metabolites, metabolic engineering, and impact of transgene(s) dissemination into managed and unmanaged plant systems.
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