381 research outputs found

    Isolation and identification of bacterial strain I33M producing milk-clotting enzyme: Optimization of culture parameters using response surface

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    A strain I33M which produces a milk-clotting enzyme was screened from Algerian soil near a dairy factory. This strain was identified as Bacillus mojavensis based on morphology and internal transcription spacer sequence. Sequencing analysis of 16S rDNA gene showed 100% identity of the tested strain with the B. mojavensis in the database. Phylogenetic analysis of this strain showed that it was most closely related to Bacillus subtilis strain. The optimum levels of these significant parameters to obtain the highest milk clotting activity and the lowest proteolytic activity were determined employing the response surface methodology (RSM), which revealed these as follows: wheat bran 7%, casein 0.094%, temperature 39°C, agitation size (rpm) 150. Among the various variables screened, agitation and temperature were most significant in submerged fermentation (SmF). The optimal value of milk clotting activity (MCA) is esteemed at 2.40. Key words: Milk clotting protease, Bacillus, response surface methodology, sequencing analysis

    Analysing cyclist behaviour at cycling facility discontinuities using video data

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    RÉSUMÉ: The primary purpose of any transportation network is to provide connectivity between the origin and travel destination. However, given the vehicle oriented structure of the road network in many countries, there are connectivity issues in the cycling network, which has been implemented later. Discontinuities are physical interruptions in the cycling network where cyclists are faced with unexpected situations such as the end of a cycling facility or the change from one facility type to another that are perceived as inconvenient and less safe. The microscopic behaviour of cyclists and the risks they face at these points of discontinuity has not been extensively investigated in the literature. This study aims to evaluate the challenges faced by cyclists at discontinuities by observing cyclist behaviour at these locations and comparing them to control sites using automated video analysis techniques. Our methodology allows the extraction of valuable microscopic data for evaluation of cyclist behaviour at any location. The methodology is applied to a case study of four sites in Montreal, Canada. Using a set of discontinuity measures proposed in a previous work and applied to Montreal’s cycling network, video data was collected from a pole-mounted camera at locations with discontinuity and control sites. After extracting road user trajectories from the video data, a trajectory clustering algorithm was applied to find cyclists’ motion patterns and the various maneuver strategies adopted by cyclists. Speeds and acceleration statistics are extracted and compared between different motion patterns and between discontinuity and control sites. Results show that cyclists undertake a larger number of maneuvers at points of discontinuity compared to their control sites, and that both cyclist accelerations and speeds exhibit larger variations at discontinuities compared to larger and more stable speeds at control sites

    G14A-06- Analysis of the DORIS, GNSS, SLR, VLBI and Gravimetric Time Series at the GGOS Core Sites

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    Analysis of the time series at the 3-4 multi-technique GGOS sites to analyze and compare the spectral content of the space geodetic and gravity time series. Evaluate the level of agreement between the space geodesy measurements and the physical tie vectors

    Nephronophthisis

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    Nephronophthisis (NPH) is an autosomal recessive disease characterized by a chronic tubulointerstitial nephritis that progress to terminal renal failure during the second decade (juvenile form) or before the age of 5 years (infantile form). In the juvenile form, a urine concentration defect starts during the first decade, and a progressive deterioration of renal function is observed in the following years. Kidney size may be normal, but loss of corticomedullary differentiation is often observed, and cysts occur usually after patients have progressed to end-stage renal failure. Histologic lesions are characterized by tubular basement membrane anomalies, tubular atrophy, and interstitial fibrosis. The infantile form is characterized by cortical microcysts and progression to end-stage renal failure before 5 years of age. Some children present with extrarenal symptoms: retinitis pigmentosa (Senior-Løken syndrome), mental retardation, cerebellar ataxia, bone anomalies, or liver fibrosis. Positional cloning and candidate gene approaches led to the identification of eight causative genes (NPHP1, 3, 4, 5, 6, 7, 8, and 9) responsible for the juvenile NPH and one gene NPHP2 for the infantile form. NPH and associated disorders are considered as ciliopathies, as all NPHP gene products are expressed in the primary cilia, similarly to the polycystic kidney disease (PKD) proteins

    The opposite of Dante's hell? The transfer of ideas for social housing at international congresses in the 1850s–1860s

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    With the advent of industrialization, the question of developing adequate housing for the emergent working classes became more pressing than before. Moreover, the problem of unhygienic houses in industrial cities did not stop at the borders of a particular nation-state; sometimes literally as pandemic diseases spread out 'transnationally'. It is not a coincidence that in the nineteenth century the number of international congresses on hygiene and social topics expanded substantially. However, the historiography about social policy in general and social housing in particular, has often focused on individual cases because of the different pace of industrial and urban development and is thus dominated by national perspectives. In this paper, I elaborate on transnational exchange processes and local adaptations and transformations. I focus on the transfer of the housing model of SOMCO in Mulhouse, (a French house building association) during social international congresses. I examine whether cross-national networking enabled and facilitated the implementation of ideas on the local scale. I will elaborate on the transmission and the local adaptation of the Mulhouse-model in Belgium. Convergences, divergences, and different factors that influenced the local transformations (personal choice, political situation, socioeconomic circumstances) will be taken into accoun

    From Physical to Virtual: Widening the Perspective on Multi-Agent Environments

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    The final publication is available at Springer via http://dx.doi.org/10.1007/978-3-319-23850-0_9Since more than a decade, the environment is seen as a key element when analyzing, developing or deploying Multi-Agent Systems (MAS) applications. Especially, for the development of multi-agent platforms it has become a key concept, similarly to many application in the area of location-based, distributed systems. An emerging, prominent application area for MAS is related to Virtual Environments. The underlying technology has evolved in a way, that these applications have grown out of science fiction novels till research papers and even real applications. Even more, current technologies enable MAS to be key components of such virtual environments. In this paper, we widen the concept of the environment of a MAS to encompass new and mixed physical, virtual, simulated, etc. forms of environments. We analyze currently most interesting application domains based on three dimensions: the way different "realities" are mixed via the environment, the underlying natures of agents, the possible forms and sophistication of interactions. In addition to this characterization, we discuss how this widened concept of possible environments influences the support it can give for developing applications in the respective domains.Carrascosa Casamayor, C.; Klugl, F.; Ricci, A.; Boissier, O. (2015). From Physical to Virtual: Widening the Perspective on Multi-Agent Environments. En Agent Environments for Multi-Agent Systems IV. 4th International Workshop, E4MAS 2014 - 10 Years Later, Paris, France, May 6, 2014. 133-146. https://doi.org/10.1007/978-3-319-23850-0_9S133146Aggarwal, J.K., Ryoo, M.S.: Human activity analysis: a review. ACM Comput. 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    Policultivo: prática agrícola de conservação on farm de fruteiras nativas da Amazônia.

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    Policultivo é uma pratica importante para manter a biodiversidade do sistema agrícola. Na Amazônia é grande a diversidade de frutas nativas, com aptidão para mesa e/ou indústria. Contudo, a maioria dessas frutíferas é desconhecida, perdendo a importância de conservação. Disponibilizar frutíferas nativas a sistemas de policultivo de espécies nativas cultivadas e culturas alimentares, contribui ao acesso da população, tornando-as conhecidas e ampliando a diversidade alimentar. Com a prática, realiza-se o resgate dessas espécies, conservando- as, evitando a erosão genética, perda das propriedades e valores nutricionais, medicinais e os sabores. No contexto, objetivou-se avaliar os resultados preliminares da prática de policultivo de espécies frutíferas nativas da Amazônia, estimulando o uso e a conservação on farm das espécies. Para tanto, instalou-se em áreas de produtores, estando o cupuaçuzeiro (Theobroma grandiflorum) e o açaizeiro (Euterpe oleracea), frutíferas nativas, ocupando 80% da área e, 20% da área com espécies frutíferas nativas não tradicionalmente cultivadas ou conhecidas de agricultores e/ou consumidores

    Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia

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    Skeletal dysplasias comprise a large spectrum of mostly monogenic disorders affecting bone growth, patterning, and homeostasis, and ranging in severity from lethal to mild phenotypes. This study aimed to underpin the genetic cause of skeletal dysplasia in three unrelated families with variable skeletal manifestations. The six affected individuals from three families had severe short stature with extreme shortening of forelimbs, short long-bones, and metatarsals, and brachydactyly (family 1); mild short stature, platyspondyly, and metaphyseal irregularities (family 2); or a prenatally lethal skeletal dysplasia with kidney features suggestive of a ciliopathy (family 3). Genetic studies by whole genome, whole exome, and ciliome panel sequencing identified in all affected individuals biallelic missense variants in KIF24, which encodes a kinesin family member controlling ciliogenesis. In families 1 and 3, with the more severe phenotype, the affected subjects harbored homozygous variants (c.1457A>G; p.(Ile486Val) and c.1565A>G; p.(Asn522Ser), respectively) in the motor domain which plays a crucial role in KIF24 function. In family 2, compound heterozygous variants (c.1697C>T; p.(Ser566Phe)/c.1811C>T; p.(Thr604Met)) were found C-terminal to the motor domain, in agreement with a genotype-phenotype correlation. In vitro experiments performed on amnioblasts of one affected fetus from family 3 showed that primary cilia assembly was severely impaired, and that cytokinesis was also affected. In conclusion, our study describes novel forms of skeletal dysplasia associated with biallelic variants in KIF24. To our knowledge this is the first report implicating KIF24 variants as the cause of a skeletal dysplasia, thereby extending the genetic heterogeneity and the phenotypic spectrum of rare bone disorders and underscoring the wide range of monogenetic skeletal ciliopathies. (c) 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).Peer reviewe

    Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization

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    Ciliopathies are a large group of clinically and genetically heterogeneous disorders caused by defects in primary cilia. Here we identified mutations in TRAF3IP1 (TNF Receptor-Associated Factor Interacting Protein 1) in eight patients from five families with nephronophthisis (NPH) and retinal degeneration, two of the most common manifestations of ciliopathies. TRAF3IP1 encodes IFT54, a subunit of the IFT-B complex required for ciliogenesis. The identified mutations result in mild ciliary defects in patients but also reveal an unexpected role of IFT54 as a negative regulator of microtubule stability via MAP4 (microtubule-associated protein 4). Microtubule defects are associated with altered epithelialization/polarity in renal cells and with pronephric cysts and microphthalmia in zebrafish embryos. Our findings highlight the regulation of cytoplasmic microtubule dynamics as a role of the IFT54 protein beyond the cilium, contributing to the development of NPH-related ciliopathies
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