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紫草科不同药用植物中含儿茶酚的生物聚合物聚[3-(3,4-二羟基苯基)甘油酸]的抗菌活性

Antimicrobial Activity of Catechol-Containing Biopolymer Poly[3-(3,4-dihydroxyphenyl)glyceric Acid] from Different Medicinal Plants of Boraginaceae Family.

作者信息

Barbakadze Vakhtang, Merlani Maia, Gogilashvili Lali, Amiranashvili Lela, Petrou Anthi, Geronikaki Athina, Ćirić Ana, Glamočlija Jasmina, Soković Marina

机构信息

TSMU I. Kutateladze Institute of Pharmacochemistry, Tbilisi 0159, Georgia.

School of Pharmacy, Aristotle University, 54124 Thessaloniki, Greece.

出版信息

Antibiotics (Basel). 2023 Feb 1;12(2):285. doi: 10.3390/antibiotics12020285.

DOI:10.3390/antibiotics12020285
PMID:36830198
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9952037/
Abstract

This study reports the antimicrobial activities of the biopolymers poly[3-(3,4-dihydoxyphenyl)glyceric acid] (PDHPGA) and poly[2-methoxycarbonyl-3-(3,4-dihydroxyphenyl)oxirane] (PMDHPO), extracted from the six plants of Boraginaceae family: (), (), and (), (), (), and () collected in various parts of Georgia. The study revealed that the antibacterial activities were moderate, and biopolymers from only three plants showed activities against all tested bacteria. Biopolymers from stems as well as and did not show any activity except low activity against a resistant strain, which was the most resistant among all three resistant strains. On the other hand, the antifungal activity was better compared to the antibacterial activity. Biopolymers from stems exhibited the best activities with MIC/MFC at 0.37-1.00 mg/mL and 0.75-1.5 mg/L, respectively, followed by those from stems. Biopolymers from and roots showed antifungal activities against all six fungi, in contrast to the antibacterial activity, while biopolymers from stems and roots had activities against four fungi and one fungus, respectively. The sugar-based catechol-containing biopolymers from stems demonstrated the best activities among all tested biopolymers against , , , and (MIC 0.37 mg/mL). In addition, biopolymers from stems were half as active against and as ketoconazole. Biopolymers from all plant materials except for stems showed higher potency than ketoconazole against For the first time, it was shown that all plant materials exhibited better activity against , one of the most dreadful fungal species.

摘要

本研究报告了从紫草科的六种植物中提取的生物聚合物聚3-(3,4-二羟基苯基)甘油酸和聚2-甲氧基羰基-3-(3,4-二羟基苯基)环氧乙烷的抗菌活性。这六种植物分别是:(此处植物名缺失)、(此处植物名缺失)、(此处植物名缺失)、(此处植物名缺失)、(此处植物名缺失)、(此处植物名缺失),采集于格鲁吉亚的不同地区。研究表明,其抗菌活性中等,只有三种植物的生物聚合物对所有测试细菌有活性。除了对一种耐药菌株有低活性外,(此处植物名缺失)茎部以及(此处植物名缺失)和(此处植物名缺失)的生物聚合物未显示出任何活性,而该耐药菌株是所有三种耐药菌株中耐药性最强的。另一方面,与抗菌活性相比,其抗真菌活性更好。(此处植物名缺失)茎部的生物聚合物表现出最佳活性,其最低抑菌浓度/最低杀菌浓度分别为0.37 - 1.00毫克/毫升和0.75 - 1.5毫克/升,其次是(此处植物名缺失)茎部的生物聚合物。与抗菌活性不同,(此处植物名缺失)和(此处植物名缺失)根部的生物聚合物对所有六种真菌均显示出抗真菌活性,而(此处植物名缺失)茎部和(此处植物名缺失)根部的生物聚合物分别对四种真菌和一种真菌有活性。(此处植物名缺失)茎部含糖基儿茶酚的生物聚合物在所有测试生物聚合物中对(此处真菌名缺失)、(此处真菌名缺失)、(此处真菌名缺失)和(此处真菌名缺失)表现出最佳活性(最低抑菌浓度为0.37毫克/毫升)。此外,(此处植物名缺失)茎部的生物聚合物对(此处真菌名缺失)和(此处真菌名缺失)的活性是酮康唑的一半。除(此处植物名缺失)茎部外,所有植物材料的生物聚合物对(此处真菌名缺失)的效力均高于酮康唑。首次表明,所有植物材料对最可怕的真菌物种之一(此处真菌名缺失)均表现出更好的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/8016ff262e04/antibiotics-12-00285-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/49592d6ace5a/antibiotics-12-00285-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/8cfaf06aa5a4/antibiotics-12-00285-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/640e05fdb30f/antibiotics-12-00285-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/828ab44feac1/antibiotics-12-00285-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/4b40fec26584/antibiotics-12-00285-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/8c7620a727f0/antibiotics-12-00285-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/8016ff262e04/antibiotics-12-00285-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/49592d6ace5a/antibiotics-12-00285-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/8cfaf06aa5a4/antibiotics-12-00285-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/640e05fdb30f/antibiotics-12-00285-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/828ab44feac1/antibiotics-12-00285-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/4b40fec26584/antibiotics-12-00285-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/8c7620a727f0/antibiotics-12-00285-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b15/9952037/8016ff262e04/antibiotics-12-00285-g007a.jpg

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