Design and testing of a cost-efficient bioremediation system for tannery effluents using native chromium-resistant filamentous fungi

In Arequipa (Peru), a small-scale tannery industry cannot afford costly or complicated methods for effluent treatment. In this work, we designed and tested a bubble column bioreactor for tannery effluent treatment based on the native filamentous fungi Penicillium citrinum and Trichoderma viride. The bioreactor construction used low-cost materials, with an easy-to-handle design. The parameters considered for testing were based on current Peruvian legislation. In the bioreactor, P. citrinum successfully reduced the effluent content of sulfides, chemical oxygen demand (COD) and total suspended solids (TSS) and removed nearly 80% of the chromium (VI) after 120 h of reaction. The resulting treated effluent had a composition within the maximum limits permitted by Peruvian legislation. Trichoderma viride also reduced the content of TSS, COD and sulfides, but decreased the chromium (VI) concentration by only ~ 20% after the same reaction time. Both filamentous fungi were able to grow in the experimental conditions used and the bioremediation process occurred with no significant alteration in pH. These findings indicate that a bubble column bioreactor using P. citrinum as a bioremediator agent provides low-cost, effective technology for treating effluent waste produced by artisanal and small-size tannery factories in the region of Arequipa1738253834This study was fnanced by UNSA-INVESTIGA (Grant No. IBA-0030-2017) and was part of an undergraduate dissertation by S.V.Z.-

Lmrtx, A Basic Pla₂ (d49) Purified From Lachesis Muta Rhombeata Snake Venom With Enzymatic-related Antithrombotic And Anticoagulant Activity.

A basic phospholipase A₂ (LmrTX) isoform was isolated from Lachesis muta rhombeata snake venom and partially characterized. The venom was fractionated by molecular exclusion chromatography in ammonium bicarbonate buffer followed by reverse-phase HPLC on a C-5 Discovery® Bio Wide column. From liquid chromatography-electrospray ionization/mass spectrometry, the molecular mass of LmrTX was measured as 14.277.50 Da. The amino acid sequence showed a high degree of homology between PLA₂ LmrTX from L. muta rhombeata and other PLA₂ from snake venoms, like CB1 and CB2 from Crotalus durissus terrificus; LmTX-I and LmTX-II from Lachesis muta muta. LmrTX had PLA₂ activity in the presence of a synthetic substrate and alkylation of histidine residues significantly inhibited (P < 0.05) the enzymatic activity of LmrTX and its anticoagulant and antithrombotic activity. In this study, we examined the ability of the LmrTX in altering thrombus formation in living mouse, using a photochemically induced arterial thrombosis model. The control animals that did not receive protein injection showed a normal occlusion time, which was around 57 ± 7.8 min. LmrTX, the PLA₂ from L. muta rhombeata venom, caused a change in the occlusion time to 99 ± 10 min with doses of 7.5 μg/mice. Additionally, LmrTX showed the anticoagulant activity in vitro and ex vivo and prolonging the time aggregation in wash platelet induced by ADP and Thrombin.60773-8