ABSTRACT
Aims@#This study was aimed to characterize a dehalogenase derived from Bacillus cereus SN1 isolated from cow dung. @*Methodology and results@#Cell-free extract of Bacillus cereus SN1 was purified using ion exchange and gel filtration chromatography. Fraction B2 of gel filtration gave the highest enzyme specific activity (0.155 μmol CI¯/min/mg). The results of SDS-PAGE showed the enzyme was 25 kDa in size. The enzyme reached its optimum activity at 30 °C at pH 6, and was inhibited by Mercury(II) sulfate (HgSO4). The Km and kcat values were 0.2 mM and 1.22/sec, respectively. The partial dehalogenase gene sequence was amplified using Group I dehalogenase primers. The amplified gene sequence was designated as DehSN1. @*Conclusion, significance and impact of study@#Dehalogenase from Bacillus cereus strain SN1 revealed new characteristics of dehalogenase protein. The findings indicated that the DehSN1 dehalogenase is a promising candidate for further studies as a bioremediation agent for agricultural applications.
ABSTRACT
Objetivo: comparar no plano sagital os efeitos esqueléticos e dentoalveolares para a maxila e mandíbula, como consequência do uso dos aparelhos Bionator, Klammt e SN1 no tratamento de más-oclusões esqueléticas Classe II. Material e métodos: foi realizado um estudo prospectivo de 21 crianças com má-oclusão esquelética de Classe II, tratadas com Bionator, Klammt ou SN1. Compararam-se mudanças no componente maxilar, mandibular e dentoalveolar através de medições e ângulos cefalométricos no plano sagital. Contrastaram-se as médias de longitudes e ângulos entre T1 e T2 pelas análises t student e wilcononox. Mediante Anova, foi contrastada a porcentagem da mudança nas medidas de interesse para os três grupos. Resultados: foram avaliadas 42 radiografias cefalométricas laterais (21 iniciais T1, 21 finais T2). Entre os participantes, 62% eram meninos e 38% eram meninas. A média das idades para início do tratamento foi 9,5 ± 1,2 anos. O SN1 apresentou a maior média de mudança na longitude mandibular Co-Pg (6,69 ± 3,3) e Co-B (6,59 ± 1,42). Encontrou-se a maior média de mudança relativa na altura do ramo mandibular no Bionator (9,52 ± 7,21). As mudanças dentoalveolares foram clinicamente relevantes para os três aparelhos. Conclusão: os aparelhos ortopédicos maxilares estimulam o crescimento mandibular sagital e vertical, controlam a posição sagital da maxila e geram mudanças dentoalveolares favoráveis para a correção de más-oclusões de Classe II.
Objective: comparing in the sagittal plane the skeletal and dento alveolar effects for the maxilla and the mandible as a result of the use of Bionator, Klammt and SN1 as a treatment of malocclusions class II skeletal. Material and Methods: a prospective study was realized on 21 boys and girls with skeletal Class II malocclusion under treatment with Bionator, Klammt or SN1, in which compare the changes in the maxillary, mandibular and dento-alveolar component by means of measurements and cephalometric angles in the sagittal plane. The averages of lengths and angles between T1y T2 was compare by t-student and wilcoxon tests. By Anova tests, contrasted the percentage of change in the measures of importance for the three groups. Results: 42 lateral skull radiographs were evaluated (21 initial-T1, 21 final-T2). 62% of participants were male and 38% were women. The average age for onset of treatment was 9.5 ± 1.2. The SN1 presented the highest average percent of change of the Co-Pg mandibular length (6.69 ± 3.3), Co-B (6.59 ± 1.42). A higher average relative change in the height of the ramus was found in Bionator (9.52 ± 7.21). Dento alveolar changes were clinically relevant for all three devices. Conclusion: orthopedic appliances stimulate mandibular sagittal and vertical growth, control the sagittal position of the maxilla, and generate favorable dento alveolar changes to correct class II malocclusions.
Subject(s)
Humans , Male , Female , Child, Preschool , Child , Orthodontic Appliances, Functional/adverse effects , Mandible , Maxilla , Malocclusion, Angle Class II/epidemiology , Malocclusion, Angle Class II/therapy , Data Interpretation, StatisticalABSTRACT
Objective:Glutamine is the main oxidative fuel of the enterocyte which enters the enterocyte primarily via amino acid transporters.The aim of the test was to study the distributions and functions of glutamine transporters in IEC-6 cell line.Methods:The rat intestinal epithelial cell line(IEC-6) was incubated in vitro.The mRNA expression of different glutamine transporters,protein expression of system ASCT2,and the [3H]-L-glutamine uptake were measured.Results:The mRNA of system ASCT2,SN1,ATA1,LAT1,LAT2 was expressed and the protein expression of ASCT2 was also validated in IEC-6.In Na+-containing buffer,the velocity of Na+-dependent glutamine uptake was(164.07?37.94) fmol/(mg protein?10min).In Na+-free buffer,the velocity of glutamine uptake was(58.71?10.51)fmol/(mg protein?10min).With the saturate dosage of MeAIB,the velocity of glutamine uptake was(81.02 ?19.59) fmol/(mg protein?10min).Conclusion:There may be five kinds of glutamine transporters(ASCT2,SN1,ATA1,LAT1,and LAT2) in IEC-6 cell.The Na+-dependent transporter was the major contributor(64.22%) to glutamine total uptake in IEC-6.The contributions of system A and the remainder were 50.62% and 13.60%,respectively.The Na+-independent transporter was the lesser contributor(35.78%).