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Three distinct biological reactors fed with synthetic medium (UASB_Control), synthetic medium and linear alkylbenzene sulfonate (LAS; UASB_SL), and real laundry wastewater (UASB_LW) were compared using a metatranscriptomic approach to determine putative bioindicator genes and taxonomies associated to all steps of anaerobic LAS biodegradation pathway. A homemade bioinformatics pipeline combined with an R workflow was developed to perform the RNAseq data analysis. UASB_SL and UASB_LW showed similar values of LAS biological degradation (~47%) and removal (53-55%). Rarefaction analysis revealed that 1-2 million reads were sufficient to access the whole functional capacity. In the first step of LAS biodegradation pathway, fumarate reductase subunit C was detected and taxonomically assigned to the genus Syntrophobacter (0.002% - UASB_SL; 0.0015% - UASB_LW; not detected - UASB_Control). In the second step, many enzymes related to beta-oxidation were observed and most of them with low relative abundance in UASB Control and taxonomically related with Smithella, Acinetobacter and Syntrophorhabdus. For the ring cleavage step, the abundance of 6 OCH CoA hydrolase putative gene was ten times higher in UASB_SL and UASB_LW when compared to UASB_Control, and assigned to Desulfomonile and Syntrophorhabdus. Finally, the adenylylsulfate reductase, taxonomically related with Desulfovibrio and Desulfomonile, was observed in the desulfonation step with the highest relative abundance in UASB_LW.

Our aims were to compare physiological parameters from the laboratory environment (LaB) and simulated goalball games (GaM), test relationships between physiological parameters in the laboratory and game technical performance (GTP), and examine the associations between physiological and technical responses during games. Seven elite athletes from the Brazilian National Team performed in LaB environment; (i) an incremental test to determine peak oxygen consumption (O2PEAK), its corresponding speed, and peak blood lactate concentration and (ii) submaximal and supramaximal efforts to estimate maximal anaerobic contribution (AnC). In GaM condition, simulated games were also performed to determine physiological responses throughout the game, and to analyze the GTP (number of throws, defenses, recovery, and density of actions). No correlations (unclear) were found between laboratory and games analyses for O2PEAK [47.3 (17.2) vs. 25.8 (18.2) mL⋅Kg-1⋅min-1], peak blood lactate concentrations [10.2 (5.4) vs. 2.0 (0.7) mM], and total AnC [21.0 (14.0) vs. 4.8 (6.1) mL Kg-1]. O2PEAK in the laboratory condition presented very likely correlations with throw and recovery frequency in games (r = -0.87 and confidence interval [CI] = 0.41; r = -0.90 and CI = 0.35; respectively). Oxygen consumption remained above baseline while blood lactate concentration remained unchanged during the games. The very likely correlation between anaerobic alactic contribution and action density (r = 0.95 and CI = 0.25) highlights the importance of the alactic metabolism. In general, our study demonstrates that goalball can be characterized as a high-intensity intermittent effort, where athlete performance is based on aerobic metabolism predominance while determinant actions are supplied by the anaerobic alactic metabolism. Specifically, higher values of LaB vs. GaM highlighted the need for standardization of specific protocols for goalball evaluation, mainly for the reproduction of ecologically valid values. In addition, O2PEAK correlated with recovery frequency in the LaB condition, demonstrating that passive or low-intensity recovery between actions is fundamental to maintain performance.

Vibrio sp. strain ABE-1 is a unique marine bacterium in terms of its ability to synthesize Δ9-trans-hexadecenoic acid and Δ7-cis-tetradecenoic acid (14:1(7c); Okuyama, H., Sasaki, S., Higashi, S. and Murata, N. (1990) J. Bacteriol. 172, 3515-3518). The present study, involving labeling with [1-14C]acetate, demonstrated that 14:1 is synthesized by the anaerobic pathway. When cells of this bacterium were grown in the presence of [1-14C]myristic acid (14:0), this compound was converted to palmitic (16:0) and hexadecenoic (16:1) acids but not to 14:1, under aerobic conditions. These results suggest that the incorporated 14:0 was elongated to 16:0 and then converted to 16:1 by the aerobic desaturation of 16:0. It appears that the anaerobic pathway and aerobic desaturation are both involved in the synthesis of unsaturated fatty acids during aerobic growth of Vibrio sp. strain ABE-1.