The Group II chaperonin from Thermoplasma acidophilum was added to the in vitro amyloid fibrillation reaction of yeast Sup35NM protein to assess its effects. By measuring the formation of Sup35NM fibrils in real time ...The Group II chaperonin from Thermoplasma acidophilum was added to the in vitro amyloid fibrillation reaction of yeast Sup35NM protein to assess its effects. By measuring the formation of Sup35NM fibrils in real time using the fluorescent dye Thioflavin T, we found that the addition of T. acidophilum-cpn α16, α1, and β1 proteins suppressed fibril formation. Addition of a 0.1 molar-equivalent T. acidophilum-cpn α16 relative to Sup35NM prolonged the initial lag-time of fibril formation and decreased the rate of fibril extension. Addition of 1 or 3 molar-equivalents of T. acidophilum-cpn monomers also produced a similar effect. Delayed addition of these chaperonins after the initial lag phase did not suppress fibril formation. Interestingly, these effects were also observed upon adding only the apical domain segments of α and β-subunits, and we also found that deletion of the helical protrusion in the apical domain of these segments led to an abolishment of the suppression effects. A synthetic peptide whose sequence corresponded to the helical protrusion also displayed a suppression effect, which indicated that archaeal group II chaperonin binds to Sup35NM through the helical protrusion of the apical domain. These findings suggest that group II chaperonin might be actively involved in suppressing amyloid fibril formation, in addition to acting as a protein folding assistant.展开更多
The aim of this research was to convert potato peel waste (PPW) to single cell protein (SCP), and to extract valuable phenolic compounds from the spent medium. PPW is an abundant by-product of potato processing indust...The aim of this research was to convert potato peel waste (PPW) to single cell protein (SCP), and to extract valuable phenolic compounds from the spent medium. PPW is an abundant by-product of potato processing industry, consisting mostly of starch, fibre and protein in a form of watery sludge. The PPW from a chip manufacturing plant was pre-treated with sulphuric acid, and used as a substrate for an acidophilic Scytalidium acidophilum fungus under non-aseptic conditions. The produced SCP had a promising amino acid composition to be used in animal feed. Phenolic compounds were not recovered from the spent medium, most likely due to the low pH in the medium. The present findings suggest that PPW is a suitable raw material for acidophilic SCP production, whilst the extraction of phenolic acids would require milder cultivation conditions or separation before pre-treatments of SCP production. The BOD5 of the PPW was reduced by in 98% due to fungal cultivation. Thus the feed production also served as an efficient means for reduction of organic load in the PPW.展开更多
文摘The Group II chaperonin from Thermoplasma acidophilum was added to the in vitro amyloid fibrillation reaction of yeast Sup35NM protein to assess its effects. By measuring the formation of Sup35NM fibrils in real time using the fluorescent dye Thioflavin T, we found that the addition of T. acidophilum-cpn α16, α1, and β1 proteins suppressed fibril formation. Addition of a 0.1 molar-equivalent T. acidophilum-cpn α16 relative to Sup35NM prolonged the initial lag-time of fibril formation and decreased the rate of fibril extension. Addition of 1 or 3 molar-equivalents of T. acidophilum-cpn monomers also produced a similar effect. Delayed addition of these chaperonins after the initial lag phase did not suppress fibril formation. Interestingly, these effects were also observed upon adding only the apical domain segments of α and β-subunits, and we also found that deletion of the helical protrusion in the apical domain of these segments led to an abolishment of the suppression effects. A synthetic peptide whose sequence corresponded to the helical protrusion also displayed a suppression effect, which indicated that archaeal group II chaperonin binds to Sup35NM through the helical protrusion of the apical domain. These findings suggest that group II chaperonin might be actively involved in suppressing amyloid fibril formation, in addition to acting as a protein folding assistant.
基金the European Regional Development Fund project A70161.
文摘The aim of this research was to convert potato peel waste (PPW) to single cell protein (SCP), and to extract valuable phenolic compounds from the spent medium. PPW is an abundant by-product of potato processing industry, consisting mostly of starch, fibre and protein in a form of watery sludge. The PPW from a chip manufacturing plant was pre-treated with sulphuric acid, and used as a substrate for an acidophilic Scytalidium acidophilum fungus under non-aseptic conditions. The produced SCP had a promising amino acid composition to be used in animal feed. Phenolic compounds were not recovered from the spent medium, most likely due to the low pH in the medium. The present findings suggest that PPW is a suitable raw material for acidophilic SCP production, whilst the extraction of phenolic acids would require milder cultivation conditions or separation before pre-treatments of SCP production. The BOD5 of the PPW was reduced by in 98% due to fungal cultivation. Thus the feed production also served as an efficient means for reduction of organic load in the PPW.
