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Keywords = PoEP1 gene

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21 pages, 6272 KB  
Article
Influence of Copper on Oleidesulfovibrio alaskensis G20 Biofilm Formation
by Payal Thakur, Vinoj Gopalakrishnan, Priya Saxena, Mahadevan Subramaniam, Kian Mau Goh, Brent Peyton, Matthew Fields and Rajesh Kumar Sani
Microorganisms 2024, 12(9), 1747; https://doi.org/10.3390/microorganisms12091747 - 23 Aug 2024
Cited by 5 | Viewed by 2530
Abstract
Copper is known to have toxic effects on bacterial growth. This study aimed to determine the influence of copper ions on Oleidesulfovibrio alaskensis G20 biofilm formation in a lactate-C medium supplemented with variable copper ion concentrations. OA G20, when grown in media supplemented [...] Read more.
Copper is known to have toxic effects on bacterial growth. This study aimed to determine the influence of copper ions on Oleidesulfovibrio alaskensis G20 biofilm formation in a lactate-C medium supplemented with variable copper ion concentrations. OA G20, when grown in media supplemented with high copper ion concentrations of 5, 15, and 30 µM, exhibited inhibited growth in its planktonic state. Conversely, under similar copper concentrations, OA G20 demonstrated enhanced biofilm formation on glass coupons. Microscopic studies revealed that biofilms exposed to copper stress demonstrated a change in cellular morphology and more accumulation of carbohydrates and proteins than controls. Consistent with these findings, sulfur (dsrA, dsrB, sat, aprA) and electron transport (NiFeSe, NiFe, ldh, cyt3) genes, polysaccharide synthesis (poI), and genes involved in stress response (sodB) were significantly upregulated in copper-induced biofilms, while genes (ftsZ, ftsA, ftsQ) related to cellular division were negatively regulated compared to controls. These results indicate that the presence of copper ions triggers alterations in cellular morphology and gene expression levels in OA G20, impacting cell attachment and EPS production. This adaptation, characterized by increased biofilm formation, represents a crucial strategy employed by OA G20 to resist metal ion stress. Full article
(This article belongs to the Special Issue Advances in Microbial Biofilm Formation)
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17 pages, 6290 KB  
Article
Functional Characterization of PoEP1 in Regulating the Flowering Stage of Tree Peony
by Yang Lei, Jingshan Gao, Yuying Li, Chengwei Song, Qi Guo, Lili Guo and Xiaogai Hou
Plants 2024, 13(12), 1642; https://doi.org/10.3390/plants13121642 - 14 Jun 2024
Cited by 4 | Viewed by 1911
Abstract
The tree peony, a traditional flower in China, has a short and concentrated flowering period, restricting the development of the tree peony industry. To explore the molecular mechanism of tree peony flowering-stage regulation, PoEP1, which regulated the flowering period, was identified and [...] Read more.
The tree peony, a traditional flower in China, has a short and concentrated flowering period, restricting the development of the tree peony industry. To explore the molecular mechanism of tree peony flowering-stage regulation, PoEP1, which regulated the flowering period, was identified and cloned based on the transcriptome and degradome data of the early-flowering mutant Paeonia ostii ‘Fengdan’ (MU) and Paeonia ostii ‘Fengdan’ (FD). Through bioinformatics analysis, expression pattern analysis, and transgene function verification, the role of PoEP1 in the regulation of tree peony flowering was explored. The open-reading frame of PoEP1 is 1161 bp, encoding 386 amino acids, containing two conserved domains. PoEP1 was homologous to the EP1 of other species. Subcellular localization results showed that the protein was localized in the cell wall and that PoEP1 expression was highest in the initial decay stage of the tree peony. The overexpression of PoEP1 in transgenic plants advanced and shortened the flowering time, indicating that PoEP1 overexpression promotes flowering and senescence and shorten the flowering time of plants. The results of this study provide a theoretical basis for exploring the role of PoEP1 in the regulation of tree peony flowering. Full article
(This article belongs to the Special Issue Floral Biology 3.0)
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