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MIKROBIELLE EINFACHTECHNOLOGIE AM BEISPIEL EINER MOBILEN PILOT-ANLAGE
No full textDie Versorgung eines Großteils der Menschheit mit Nahrungsmitteln
in Form von Protein stellt schon heute ein Problem dar. Die Lösung i
dieser Aufgabe wird aufgrund der Bevölkerungsentwicklung in vielen
Ländern immer größere Anstrengungen erfordern. Eine gewisse Ent- i lastung im Kampf gegen das Nahrungsmitteldefizit wird durch neuere |
Erkenntnis auf dem Gebiet der Mikrobiologie erwirkt. So können heute i
Mikroorganismen in industriellem Maßstab produziert werden, die über
den Umweg des Nutztieres dem Menschen zugute kommen. Wesentliche Vor- }
teile in dieser Nahrungskette sind die geringeren Verluste, die kürzeren
Produktionszeiten und die höhere Wertigkeit
ANALYTISCHE CHARAKTERISIERUNG VON NICHT-PROTEINARTIGEN BEGLEITSTOFFEN IN EINEM SCP (METHYLOMONAS CLARA)
No full textAnalytical profile of non protein compounds in a SCP (M. clara)
In different batches of a single cell protein (Methylomonas clara, Fa.
Hoechst) the lipid fraction as well as the nucleic acid fraction were
characterised by analytical means.
65 % of the extracted lipid fraction were phospholipids, 15 % were
neutral lipids and 20 % were glycolipids. The unsaponifiable part was
1,4 %, polyhydroxybutyrate (PHP) was not detected. Unusual fatty acids
as cyclopropane- or cyclopropene fatty acids were absent. The fatty
acid profile revealed that 80-90 3 were Cıg-fatty acids.
The content of free bases in the nucleic acid fraction was surprisingly
high, this is probably due to a cleavage of RNA during the technical
processing of the bacterial product. Switching from batch fermentation
to continuous fermentation resulted in a significant decrease of the
RNA content.
By a special two stage extraction procedure a protein concentrate is
obtained which containes only small amounts of lipids and nucleic acids.
This product is of much higher nutritional value
Three novel Rubripirellula species isolated from plastic particles submerged in the Baltic Sea and the estuary of the river Warnow in northern Germany.
No full textPlanctomycetes are a unique and important phylum containing mostly aquatic bacteria, which are often associated with phototrophic surfaces. A complex lifestyle, their potential for the production of bioactive small molecules, their unusual cell biology and a large number of giant and hypothetical genes in their genomes make these microorganisms a fascinating topic for further research. Here, we characterise three novel planctomycetal strains isolated from polystyrene and polyethylene particles that were submerged in the German part of the Baltic Sea and the estuary of the river Warnow. All three strains showed typical planctomycetal traits such as division by polar budding and formation of rosettes. The isolated strains were mesophilic and neutrophilic chemoheterotrophs and reached generation times of 10-25 h during laboratory-scale cultivation. Taxonomically, the three strains belong to the genus Rubripirellula. Based on our analyses all three strains represent novel species, for which we propose the names Rubripirellula amarantea sp. nov., Rubripirellula tenax sp. nov. and Rubripirellula reticaptiva sp. nov. The here characterised strains Pla22T (DSM 102267T = LMG 29691T), Poly51T (DSM 103356T = VKM B-3438T) and Poly59T (DSM 103767T = LMG 29696T) are the respective type strains of these novel species. We also emend the description of the genus Rubripirellula
LOW COST DATA ACQUISITION AND ANALYSIS WITH ON-LINE DESK CALCULATORS
No full textA low cost version for the interfacing of a programmable
desk calculator to a well instrumented fermentation system
is described providing the possibilities of data
acquisition and on-line as well as off-line data analysis
with high efficiency and flexibility, which enables
also smaller research units to perform advanced fermentation
research on the laboratory or pilot-plant scale.
Further advantages of the present configuration are the
ease of programming and the versatility of almost every
part of the system
MicroRNA-342-3p is a potent tumour suppressor in hepatocellular carcinoma
No full textBackground & aims: Hepatocellular carcinoma (HCC) is a cancer with multiple aetiologies and widespread prevalence. Largely refractory to current treatments, HCC is the fourth leading cause of cancer-related deaths worldwide. MicroRNAs (miRNAs) are important regulators in HCCs. We aimed to identify tumour suppressor miRNAs during tumour regression in a conditional c-MYC-driven mouse model (LT2/MYC) of HCC, and to evaluate their therapeutic potential for HCC treatment.
Methods: We performed miRNA expression profiling of developed and regressing LT2/MYC tumours and in-depth in vitro gain- and loss-of-function analyses. The effect of adeno-associated virus (AAV) vector-mediated miR-342-3p treatment was evaluated in 3 HCC mouse models.
Results: We identified miR-342-3p as a tumour suppressor miRNA in HCC, with increased expression in regressing tumours. Forced miR-342-3p expression in hepatoma cells showed significantly decreased cell proliferation, migration, and colony formation. In vivo administration of AAV-miR-342-3p led to significant attenuation of tumour development and increased overall survival. We identified monocarboxylic acid transporter 1 (MCT1) as a bona fide target of miR-342-3p in HCC. We show that the tumour suppressor role of miR-342-3p is executed partly by modulating the lactate transport function of MCT1. Importantly, we find miR-342-3p downregulated in tumours from patients with HCC compared with matched non-tumour tissues, inversely correlating with MCT1 expression. We observed similar findings in TCGA-LIHC data.
Conclusions: In our study, we identified and validated miR-342-3p as a tumour suppressor miRNA in HCC. We demonstrated its therapeutic efficacy in significantly attenuating tumour development, and prolonging survival, in different HCC mouse models. Identification of miR-342-3p as an effective tumour suppressor opens a therapeutic avenue for miRNA-mediated attenuation of HCC development.
Lay summary: Hepatocellular carcinoma (HCC), the most common type of liver cancer, affects diverse populations and has a global impact, being the fourth leading cause of cancer deaths worldwide. There are currently no systemic therapies for HCC that can significantly prolong long-term survival. Thus, novel effective treatment options are urgently required. To understand the molecular basis of tumour regression, we compared tumours and regressing liver tumours in mice. We show that a small non-coding miRNA, miR-342-3p, is a tumour suppressor in HCC. Expression of miR-342-3p is low in tumours and high in regressing tumours. When miR-342-3p is delivered to mouse livers with HCC, it can significantly slow down liver tumour development and improve survival. Our study highlights the promising therapeutic potential of miR-342-3p intervention in HCC.Deutsche Krebshilf
Cyclin D3 drives inertial cell cycling in dark zone germinal center B cells.
No full textDuring affinity maturation, germinal center (GC) B cells alternate between proliferation and somatic hypermutation in the dark zone (DZ) and affinity-dependent selection in the light zone (LZ). This anatomical segregation imposes that the vigorous proliferation that allows clonal expansion of positively selected GC B cells takes place ostensibly in the absence of the signals that triggered selection in the LZ, as if by "inertia." We find that such inertial cycles specifically require the cell cycle regulator cyclin D3. Cyclin D3 dose-dependently controls the extent to which B cells proliferate in the DZ and is essential for effective clonal expansion of GC B cells in response to strong T follicular helper (Tfh) cell help. Introduction into the Ccnd3 gene of a Burkitt lymphoma-associated gain-of-function mutation (T283A) leads to larger GCs with increased DZ proliferation and, in older mice, clonal B cell lymphoproliferation, suggesting that the DZ inertial cell cycle program can be coopted by B cells undergoing malignant transformation
Initial HCV infection of adult hepatocytes triggers a temporally structured transcriptional program containing diverse pro- and anti-viral elements.
No full textTranscriptional profiling provides global snapshots of virus-mediated cellular reprogramming, which can simultaneously encompass pro- and antiviral components. To determine early transcriptional signatures associated with HCV infection of authentic target cells, we performed ex vivo infections of adult primary human hepatocytes (PHHs) from seven donors. Longitudinal sampling identified minimal gene dysregulation at six hours post infection (hpi). In contrast, at 72 hpi, massive increases in the breadth and magnitude of HCV-induced gene dysregulation were apparent, affecting gene classes associated with diverse biological processes. Comparison with HCV-induced transcriptional dysregulation in Huh-7.5 cells identified limited overlap between the two systems. Of note, in PHHs, HCV infection initiated broad upregulation of canonical interferon (IFN)-mediated defense programs, limiting viral RNA replication and abrogating virion release. We further find that constitutive expression of IRF1 in PHHs maintains a steady-state antiviral program in the absence of infection, which can additionally reduce HCV RNA translation and replication. We also detected infection-induced downregulation of ∼90 genes encoding components of the EIF2 translation initiation complex and ribosomal subunits in PHHs, consistent with a signature of translational shutoff. As HCV polyprotein translation occurs independently of the EIF2 complex, this process is likely pro-viral: only translation initiation of host transcripts is arrested. The combination of antiviral intrinsic and inducible immunity, balanced against pro-viral programs, including translational arrest, maintains HCV replication at a low-level in PHHs. This may ultimately keep HCV under the radar of extra-hepatocyte immune surveillance while initial infection is established, promoting tolerance, preventing clearance and facilitating progression to chronicity.IMPORTANCEAcute HCV infections are often asymptomatic and therefore frequently undiagnosed. We endeavored to recreate this understudied phase of HCV infection using explanted PHHs and monitored host responses to initial infection. We detected temporally distinct virus-induced perturbations in the transcriptional landscape, which were initially narrow but massively amplified in breadth and magnitude over time. At 72 hpi, we detected dysregulation of diverse gene programs, concurrently promoting both virus clearance and virus persistence. On the one hand, baseline expression of IRF1 combined with infection-induced upregulation of IFN-mediated effector genes suppresses virus propagation. On the other, we detect transcriptional signatures of host translational inhibition, which likely reduces processing of IFN-regulated gene transcripts and facilitates virus survival. Together, our data provide important insights into constitutive and virus-induced transcriptional programs in PHHs, and identifies simultaneous antagonistic dysregulation of pro-and anti-viral programs which may facilitate host tolerance and promote viral persistence
An extended catalogue of tandem alternative splice sites in human tissue transcriptomes.
No full textTandem alternative splice sites (TASS) is a special class of alternative splicing events that are characterized by a close tandem arrangement of splice sites. Most TASS lack functional characterization and are believed to arise from splicing noise. Based on the RNA-seq data from the Genotype Tissue Expression project, we present an extended catalogue of TASS in healthy human tissues and analyze their tissue-specific expression. The expression of TASS is usually dominated by one major splice site (maSS), while the expression of minor splice sites (miSS) is at least an order of magnitude lower. Among 46k miSS with sufficient read support, 9k (20%) are significantly expressed above the expected noise level, and among them 2.5k are expressed tissue-specifically. We found significant correlations between tissue-specific expression of RNA-binding proteins (RBP), tissue-specific expression of miSS, and miSS response to RBP inactivation by shRNA. In combination with RBP profiling by eCLIP, this allowed prediction of novel cases of tissue-specific splicing regulation including a miSS in QKI mRNA that is likely regulated by PTBP1. The analysis of human primary cell transcriptomes suggested that both tissue-specific and cell-type-specific factors contribute to the regulation of miSS expression. More than 20% of tissue-specific miSS affect structured protein regions and may adjust protein-protein interactions or modify the stability of the protein core. The significantly expressed miSS evolve under the same selection pressure as maSS, while other miSS lack signatures of evolutionary selection and conservation. Using mixture models, we estimated that not more than 15% of maSS and not more than 54% of tissue-specific miSS are noisy, while the proportion of noisy splice sites among non-significantly expressed miSS is above 63%
Understanding the interaction between cytomegalovirus and tuberculosis in children: The way forward.
No full textOver 1 million children develop tuberculosis (TB) each year, with a quarter dying. Multiple factors impact the risk of a child being exposed to Mycobacterium tuberculosis (Mtb), the risk of progressing to TB disease, and the risk of dying. However, an emerging body of evidence suggests that coinfection with cytomegalovirus (CMV), a ubiquitous herpes virus, impacts the host response to Mtb, potentially influencing the probability of disease progression, type of TB disease, performance of TB diagnostics, and disease outcome. It is also likely that infection with Mtb impacts CMV pathogenesis. Our current understanding of the burden of these 2 diseases in children, their immunological interactions, and the clinical consequence of coinfection is incomplete. It is also unclear how potential interventions might affect disease progression and outcome for TB or CMV. This article reviews the epidemiological, clinical, and immunological literature on CMV and TB in children and explores how the 2 pathogens interact, while also considering the impact of HIV on this relationship. It outlines areas of research uncertainty and makes practical suggestions as to potential studies that might address these gaps. Current research is hampered by inconsistent definitions, study designs, and laboratory practices, and more consistency and collaboration between researchers would lead to greater clarity. The ambitious targets outlined in the World Health Organization End TB Strategy will only be met through a better understanding of all aspects of child TB, including the substantial impact of coinfections