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Frydman, C.

Publications and source records attributed to Frydman, C..

2 recordsLinked to original sources

PMA-qPCR: ACCELERATING THE MARKET RELEASE OF HIGH-QUALITY BRADYRHIZOBIUM DIAZOEFFICIENS INOCULANTS

The quantification of Bradyrhizobium diazoefficiens in inoculants traditionally relies on culture-based assays, which are labor-intensive and time-consuming. To address this limitation, we validated a PMA-qPCR assay as a rapid and reliable alternative for estimating viable Bradyrhizobium counts. The assay demonstrated strong performance, achieving approximately 95% efficiency, a standard deviation of 0.3 log CFU/ml, and an intra-assay reproducibility with a coefficient of variation less than 10%. Key experiments optimized PMA concentration to ensure selective exclusion of non-viable cells without compromising viable cell quantification. Discrimination threshold assessment confirmed the assays ability to differentiate quarter-strength dilutions. Final validation against plate counting revealed an 82% correlation, significantly reducing processing time from 120 hours to just 5 hours. This is the first study to apply PMA-qPCR specifically for Bradyrhizobium diazoefficiens quantification in inoculants. The results highlight its potential as a high-throughput tool for microbial viability assessment, offering improvements in efficiency and precision for batch-to-batch quality control in industrial applications.

microbiology↗

Screening for New Interaction Partners for a Group IIB Intron Ribozyme with Surface Plasmon Resonance Imaging Coupled to MALDI Mass Spectrometry

We coupled SPR imaging (SPRi) with matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) to identify new potential RNA binders. Here, we improve this powerful method, especially by optimizing the proteolytic digestion (type of reducing agent, its concentration, and incubation time), to work with complex mixtures, specifically a lysate of the rough mitochondrial fraction from yeast. The advantages of this hyphenated method compared to column-based or separate analyses are (i) rapid and direct visual readout from the SPRi array, (ii) possibility of high-throughput analysis of different interactions in parallel, (iii) high sensitivity, and (iv) no sample loss or contamination due to elution or micro-recovery procedures. The model system used is a catalytically active RNA (group IIB intron from Saccharomyces cerevisiae, Sc.ai5{gamma}) and its cofactor Mss116. The protein supports the RNA folding process and thereby the subsequent excision of the intronic RNA from the coding part. Using the novel approach of coupling SPR with MALDI MS, we report the identification of potential RNA-binding proteins from a crude yeast mitochondrial lysate in a non-targeted approach. Our results show that proteins other than the well-known cofactor Mss116 interact with Sc.ai5{gamma} (Dbp8, Prp8, Mrp13, and Cullin-3), suggesting that the intron folding and splicing are regulated by more than one cofactor in vivo. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=141 SRC="FIGDIR/small/082776v3_ufig1.gif" ALT="Figure 1"> View larger version (20K): org.highwire.dtl.DTLVardef@50a09borg.highwire.dtl.DTLVardef@1602253org.highwire.dtl.DTLVardef@6d9cc7org.highwire.dtl.DTLVardef@4ff0f0_HPS_FORMAT_FIGEXP M_FIG C_FIG Author contributionUlrike Anders and Maya Gulotti-Georgieva contributed equally to this work.

molecular biology↗