BUSCADOR RECOLECTA

Histone methyltransferases are co-expressed and correlate with NNMT/PEMT orthologues/analogues in C. elegans., Peer reviewed

Highly expressed histone methyltransferase genes are co-expressed., Peer reviewed

NNMT expression anticorrelate globally with levels of specific histone marks genome-wide in cancer cell lines (related to Fig 3)., Peer reviewed

PEMT expression anticorrelate globally with levels of specific histone marks genome-wide in healthy tissues (related to Fig 3)., Peer reviewed

2 tables, 2 figures, Supporting information for the article https://doi.org/10.3390/su14116472, Table S1 – Relative abundance of molecular species of fatty acids (expressed as % of total pool of fatty acids) of Hermetia illucens larvae fed with different substrates retrieved from the literature surveyed.-- Table S2: Dataset used on MetaboAnalist to perform the statistical analysis.-- Table S3 - Top 10 peer-reviewed scientific journals publishing scientific research addressing the fatty acid profile of Hermetia illucens retrieved from WoS™ and Scopus. (Journals publishing 5 or less articles on this topic were grouped as Others).-- Figure S1: Box plots and kernel density plots before and after normalization. The boxplots show at most 50 features due to space limitations. The density plots are based on all samples. Data transformation: Log Normalization; Data scaling: Autoscaling.-- Figure S2: Hierarchical clustering of substrates shown as dendrogram (distance measures using Euclidean, and clustering algorithm using Ward’s Distance).-- References, Peer reviewed

[Description of methods used for collection/generation of data] Meteorological and limnological methodologies., Peer reviewed

Experimental appendix including photophysical and computational methods and X-ray crystallography details (2299209–2299212); NMR spectra and X-ray diffraction figures for structural characterization; theoretical calculations; and photophysical properties., Cartesian coordinates of the DFT-optimized structures for complexes 1, 2, 1-Cl, 1-I, and [{Pt(bzq)(μ-S∧N)2}] (HS∧N = 2-mercaptopyrimidine)., Peer reviewed

-Additional experimental details, NMR data, and methods and computational details (PDF). -Cartesian coordinates of computed structures (XYZ)., Peer reviewed

1 figure, 3 tables, Supporting information for the article https://doi.org/10.1016/j.wasman.2022.01.035, Figure S1 - Box plots and kernel density plots before and after normalization. The density plots are based on all samples. Data transformation: Log Normalization; Data scaling: Autoscaling.-- Table S1 – Amino acids content from substrates of the five study groups: control group (a), 25% replacement (b), 50% replacement (c), 75% replacement (d) and 100% replacement (e)) of expired fish feed. (g/100 g total amino acids). OHPro: hydroxyproline. Errors are the confidence intervals for n=2 (replicates of analysis) and α =0.05.-- Table S2 – Amino acids content of Black Soldier Fly larvae (g/100 g total amino acids). Errors are the confidence intervals for n=2 (replicates of analysis) and α=0.05.-- Table S3 - Fatty acid composition from substrates lipid extracts of the five study groups: control group (a), 25% replacement (b), 50% replacement (c), 75% replacement (d) and 100% replacement (e) of expired fish feed. Abundances are expressed in relative abundance (%) and values are means of five samples (n = 5) ± standard deviation, Peer reviewed

Electronic supplementary material, Figure S1. Box plot of the α-diversity index Observed richness for the bacterial community at each sampling time (0, 15, 30, 50 days after bacterization) of control (CON), V. dahliae-inoculated (Vd), Pseudomonas simiae–treated (PICF7), P. simiae PICF7/V. dahliae-inoculated (PICF7_Vd), P. polymyxa-treated (PIC73) and P. polymyxa/V. dahliae-inoculated (PIC73_Vd) plants. The statistical differences resulted by the Dunn post-hoc test are represented by asterisks (level of significance: *p < 0.05; **p < 0.01; ***p < 0.001). Figure S2. Box plot of the α-diversity indices Observed richness for the fungal community at each sampling time (0, 15, 30, 50 days after bacterization) of control (CON), V. dahliae-inoculated (Vd), Pseudomonas simiae–treated (PICF7), P. simiae/ V. dahliae-inoculated (PICF7_Vd), P. polymyxa-treated (PIC73) and P. polymyxa/ V. dahliae-inoculated (PIC73_Vd) plants. The statistical differences resulted by the Dunn post-hoc test are represented by asterisks (level of significance: *p < 0.05; **p < 0.01; ***p < 0.001). Figure S3. PCoA analysis with the Weighted-Unifrac distance of control (CON), V. dahliae-inoculated (Vd), Pseudomonas simiae–treated (PICF7), P. simiae/ V. dahliae-inoculated (PICF7_Vd), P. polymyxa-treated (PIC73) and P. polymyxa/ V. dahliae-inoculated (PIC73_Vd) plants. Figure S4. PCoA analysis of the bacterial community with the Weighted-Unifrac distance for the bacterial community at each sampling time (0, 15, 30, 50 days after bacterization) of control (CON), V. dahliae-inoculated (Vd), Pseudomonas simiae–treated (PICF7), P. simiae/ V. dahliae-inoculated (PICF7_Vd), P. polymyxa-treated (PIC73) and P. polymyxa/ V. dahliae-inoculated (PIC73_Vd) plants. Figure S5. PCoA analysis with the Weighted-Unifrac distance for the factor “time” considering all the sampling times: zero (0), fifteen (15), thirty (30) and fifty (50) days after bacterization. Figure S6. PCoA analysis with Bray Curtis distance for the factor “time” considering all the sampling times: zero (0), fifteen (15), thirty (30) and fifty (50) days after bacterization. Figure S7. Taxonomy profiles at phylum level of the olive ‘Picual’ root-associated microbiota upon treatment with two biological control agents and in the absence or presence (subsequent inoculation) of Verticillium dahliae. Bacterial (A) and fungal (B) communities at phylum level for the different treatments examined: control (CON), Paenibacillus polymyxa-treated (PIC73), P. polymyxa/V. dahliae-inoculated (PIC73_Vd), Pseudomonas simiae-treated (PICF7), P. simiae/V. dahliae-inoculated (PICF7_Vd) and V. dahliae-inoculated (Vd) plants. Only the phyla with relative abundance > 1% for bacteria and 0.1% for fungi are shown (n = 10). Asterisks indicate the phyla that showed significant differences (ANCOMB p < 0.05) by the taxonomical analysis (see the main text). Figure S8. Taxonomy profiles at phylum level of the olive ‘Picual’ root-associated microbiota upon treatment with two biological control agents and in the absence or presence (subsequent inoculation) of Verticillium dahliae at each sampling time (0, 15, 30, 50 days after bacterization). Bacterial (A) and fungal (B) communities at phylum level for the different treatments examined: control (CON), Paenibacillus polymyxa-treated (PIC73), P. polymyxa/V. dahliae-inoculated (PIC73_Vd), Pseudomonas simiae-treated (PICF7), P. simiae/V. dahliae-inoculated (PICF7_Vd) and V. dahliae-inoculated (Vd) plants. Only the genera with relative abundance > 1% for bacteria and 0.1% for fungi are shown (n = 10). Figure S9. Taxonomic profiles at genus level of the bacterial community at each sampling time (0, 15, 30, 50 days after bacterization) of control (CON), Paenibacillus polymyxa-treated (PIC73), P. polymyxa/V. dahliae-inoculated (PIC73_Vd), Pseudomonas simiae-treated (PICF7), P. simiae/V. dahliae-inoculated (PICF7_Vd) and V. dahliae-inoculated (Vd) plants. Only the genera with a relative abundance > 2% are shown (n = 10). Asterisks indicate the genera that showed significant differences (ANCOMB p < 0.05) by the taxonomical analysis (see the main text). Figure S10. Taxonomic profiles at genus level of the fungal community at each sampling time (0, 15, 30, 50 days after bacterization) of control (CON), Paenibacillus polymyxa-treated (PIC73), P. polymyxa/V. dahliae-inoculated (PIC73_Vd), Pseudomonas simiae-treated (PICF7), P. simiae/V. dahliae-inoculated (PICF7_Vd) and V. dahliae-inoculated (Vd) plants. Only the genera with a relative abundance > 2% are shown (n = 10). Asterisk indicates the genus that showed significant differences (ANCOMB p < 0.05by the taxonomical analysis (see the main text)., Peer reviewed