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qRT-PCR analysis of <t>acgfp1</t> relative expression levels in Rosetta-P ( A ), Rosetta-P efp ( B ), Rosetta-P efp110 ( C ), Rosetta-P efp135 ( D ), Rosetta-P efp145 ( E ) and Rosetta-N ( F ). Each strain was analyzed with three biological replicates, and during the qRT-PCR, three technical replicates were used for each biological replicate. Bacterial cells for acgfp1 expression analysis were cultured at 37 °C with shaking at 200 r/min for 24 h. qRT-PCR data were calculated using the ΔΔCt method, with relative expression levels quantified as 2. −ΔΔCt . The standard deviation in each group was calculated using the STDEPV function in Excel, and significance analysis was performed using one-way analysis of variance in SPSS software. Error bars represent standard deviation, “*” means statistical significance ( P < 0.05), “**” means statistical significance ( P < 0.01)
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qRT-PCR analysis of acgfp1 relative expression levels in Rosetta-P ( A ), Rosetta-P efp ( B ), Rosetta-P efp110 ( C ), Rosetta-P efp135 ( D ), Rosetta-P efp145 ( E ) and Rosetta-N ( F ). Each strain was analyzed with three biological replicates, and during the qRT-PCR, three technical replicates were used for each biological replicate. Bacterial cells for acgfp1 expression analysis were cultured at 37 °C with shaking at 200 r/min for 24 h. qRT-PCR data were calculated using the ΔΔCt method, with relative expression levels quantified as 2. −ΔΔCt . The standard deviation in each group was calculated using the STDEPV function in Excel, and significance analysis was performed using one-way analysis of variance in SPSS software. Error bars represent standard deviation, “*” means statistical significance ( P < 0.05), “**” means statistical significance ( P < 0.01)

Journal: BMC Microbiology

Article Title: Expression of translation elongation factor P in Kocuria rhizophila is regulated by an inducible weak promoter

doi: 10.1186/s12866-026-04860-9

Figure Lengend Snippet: qRT-PCR analysis of acgfp1 relative expression levels in Rosetta-P ( A ), Rosetta-P efp ( B ), Rosetta-P efp110 ( C ), Rosetta-P efp135 ( D ), Rosetta-P efp145 ( E ) and Rosetta-N ( F ). Each strain was analyzed with three biological replicates, and during the qRT-PCR, three technical replicates were used for each biological replicate. Bacterial cells for acgfp1 expression analysis were cultured at 37 °C with shaking at 200 r/min for 24 h. qRT-PCR data were calculated using the ΔΔCt method, with relative expression levels quantified as 2. −ΔΔCt . The standard deviation in each group was calculated using the STDEPV function in Excel, and significance analysis was performed using one-way analysis of variance in SPSS software. Error bars represent standard deviation, “*” means statistical significance ( P < 0.05), “**” means statistical significance ( P < 0.01)

Article Snippet: pET-32a(+)- acgfp1 , pET-32a(+) harboring the acgfp1 , Synthesized by Sangon Biotech (Shanghai) Co., Ltd.

Techniques: Quantitative RT-PCR, Expressing, Cell Culture, Standard Deviation, Software

qRT-PCR analysis of acgfp1 relative expression level in recombinant K. rhizophila strains of KR-P ( A ), KR-P efp ( B ), KR-P efp110 ( C ), KR-P efp135 ( D ), KR-P efp145 ( E ) and KR-N ( F ). Each strain was analyzed with three biological replicates, and during the qRT-PCR, three technical replicates were used for each biological replicate. Bacterial cells for acgfp1 expression analysis were cultured at 30 °C with shaking at 200 r/min for 24 h. qRT-PCR data were calculated using the ΔΔCt method, with relative expression levels quantified as 2. −ΔΔCt . The standard deviation in each group was calculated using the STDEPV function in Excel, and significance analysis was performed using one-way analysis of variance in SPSS software. Error bars represent standard deviation, “*” means statistical significance ( P < 0.05), “**” means statistical significance ( P < 0.01)

Journal: BMC Microbiology

Article Title: Expression of translation elongation factor P in Kocuria rhizophila is regulated by an inducible weak promoter

doi: 10.1186/s12866-026-04860-9

Figure Lengend Snippet: qRT-PCR analysis of acgfp1 relative expression level in recombinant K. rhizophila strains of KR-P ( A ), KR-P efp ( B ), KR-P efp110 ( C ), KR-P efp135 ( D ), KR-P efp145 ( E ) and KR-N ( F ). Each strain was analyzed with three biological replicates, and during the qRT-PCR, three technical replicates were used for each biological replicate. Bacterial cells for acgfp1 expression analysis were cultured at 30 °C with shaking at 200 r/min for 24 h. qRT-PCR data were calculated using the ΔΔCt method, with relative expression levels quantified as 2. −ΔΔCt . The standard deviation in each group was calculated using the STDEPV function in Excel, and significance analysis was performed using one-way analysis of variance in SPSS software. Error bars represent standard deviation, “*” means statistical significance ( P < 0.05), “**” means statistical significance ( P < 0.01)

Article Snippet: pET-32a(+)- acgfp1 , pET-32a(+) harboring the acgfp1 , Synthesized by Sangon Biotech (Shanghai) Co., Ltd.

Techniques: Quantitative RT-PCR, Expressing, Recombinant, Cell Culture, Standard Deviation, Software

P154 in PVY CP is a key binding site for PVY CP (A) Three-dimensional view of molecular docking of D13 . (B) Planar view of molecular docking of D13 . (C–H) MST results of PVY CP and mutant protein PVY CP P154A with compound D13 , RBV and NNM.

Journal: iScience

Article Title: Sulfonamine-containing aurone derivatives act as inhibitors of intercellular movement of potato virus Y

doi: 10.1016/j.isci.2025.113914

Figure Lengend Snippet: P154 in PVY CP is a key binding site for PVY CP (A) Three-dimensional view of molecular docking of D13 . (B) Planar view of molecular docking of D13 . (C–H) MST results of PVY CP and mutant protein PVY CP P154A with compound D13 , RBV and NNM.

Article Snippet: pET-32a(+) PVY CP P154A prokaryotic expression plasmid , Sangon Biotech , Custom synthesis, https://www.sangon.com.

Techniques: Binding Assay, Mutagenesis