关于（荒野）殖民化

由于人类体验自然的渴望日益增长,在政治和实践层面,在城市中提供接触自然的机会显得越来越必要。关于“城市荒野”的思想和规划旨在提供一种特殊的自然体验。鉴于不同荒野思想之间存在冲突,风景园林师必须设法了解已有的荒野认知及其含义。通过 3 个荒野类别—“未知荒野”“特定荒野”和“过程荒野”,探讨发展千年的荒野理念,并提出“殖民化”（colonisations）概念作为理解荒野理念发展的一个关键。自然过程伴随着动植物对空间的殖民,而人类进入和占有空间的殖民过程则包含生理、心理和精神 3 个层面的内容。空间命名是一种特殊的、具有精神和象征意味的殖民化形式。例如,人类在城市中发现野生植被,称其为“野性自然”或“城市荒野”。然而,如今大多数（尤其官方）的荒野定义中均排除了人类干扰：一旦被殖民,真正的荒野就不复存在。科学研究对自然过程的殖民化已取得很多成果,但对于人类有关自然和荒野的认知和态度了解并不多。对于风景园林师来说,这有助于更好地理解如何“基于自然进行设计和建造”,对创造令人满意的景观也非常重要。探讨与“城市荒野”有关的论述、规划和设计观点及思想。 由于人类体验自然的渴望日益增长,在政治和实践层面,在城市中提供接触自然的机会显得越来越必要。关于“城市荒野”的思想和规划旨在提供一种特殊的自然体验。鉴于不同荒野思想之间存在冲突,风景园林师必须设法了解已有的荒野认知及其含义。通过 3 个荒野类别—“未知荒野”“特定荒野”和“过程荒野”,探讨发展千年的荒野理念,并提出“殖民化”（colonisations）概念作为理解荒野理念发展的一个关键。自然过程伴随着动植物对空间的殖民,而人类进入和占有空间的殖民过程则包含生理、心理和精神 3 个层面的内容。空间命名是一种特殊的、具有精神和象征意味的殖民化形式。例如,人类在城市中发现野生植被,称其为“野性自然”或“城市荒野”。然而,如今大多数（尤其官方）的荒野定义中均排除了人类干扰：一旦被殖民,真正的荒野就不复存在。科学研究对自然过程的殖民化已取得很多成果,但对于人类有关自然和荒野的认知和态度了解并不多。对于风景园林师来说,这有助于更好地理解如何“基于自然进行设计和建造”,对创造令人满意的景观也非常重要。探讨与“城市荒野”有关的论述、规划和设计观点及思想。     

Ribosomal protein RPL22/eL22 regulates the cell cycle by acting as an inhibitor of the CDK4-cyclin D complex

Senescence is a tumor suppressor program characterized by a stable growth arrest while maintaining cell viability. Senescence-associated ribogenesis defects (SARD) have been shown to regulate senescence through the ability of the ribosomal protein S14 (RPS14 or uS11) to bind and inhibit the cyclin-dependent kinase 4 (CDK4). Here we report another ribosomal protein that binds and inhibits CDK4 in senescent cells: L22 (RPL22 or eL22). Enforcing the expression of RPL22/eL22 is sufficient to induce an RB and p53-dependent cellular senescent phenotype in human fibroblasts. Mechanistically, RPL22/eL22 can interact with and inhibit CDK4-Cyclin D1 to decrease RB phosphorylation both in vitro and in cells. Briefly, we show that ribosome-free RPL22/eL22 causes a cell cycle arrest which could be relevant during situations of nucleolar stress such as cellular senescence or the response to cancer chemotherapy.     

Monitoring gradient formation in a jet aerated bioreactor

Jet aerated loop reactors (JLRs) provide high mass transfer coefficients (k_La) and can be used for the intensification of mass transfer limited reactions. The jet loop reactor achieves higher k_La values than a stirred tank reactor (STR). The improvement relies on significantly higher local power inputs (～10⁴) than those obtainable with the STR. Operation at high local turnover rates requires efficient macromixing, otherwise reactor inhomogeneities might occur. If sufficient homogenization is not achieved, the selectivity of the reaction and the respective yields are decreased. Therefore, the balance between mixing and mass transfer in jet loop reactors is a critical design aspect. Monitoring the dissolved oxygen levels during the turnover of a steady sodium sulfite feed implied the abundance of gradients in the JLR. Prolonged mixing times at identical power input and aeration rates (～100%) were identified for the JLR in comparison to the STR. The insertion of a draft tube to the JLR led to a more homogenous dissolved oxygen distribution, but unfortunately a reduction of mixing time was not achieved. In case of increased medium viscosities as they may arise in high cell density cultivations, no gradient formation was detected. However, differences in medium viscosity significantly altered the mass transfer and mixing performance of the JLR.     

Mdm10 is an ancient eukaryotic porin co-occurring with the ERMES complex

Mitochondrial β-barrel proteins fulfill central functions in the outer membrane like metabolite exchange catalyzed by the voltage-dependent anion channel (VDAC) and protein biogenesis by the central components of the preprotein translocase of the outer membrane (Tom40) or of the sorting and assembly machinery (Sam50). The mitochondrial division and morphology protein Mdm10 is another essential outer membrane protein with proposed β-barrel fold, which has so far only been found in Fungi. Mdm10 is part of the endoplasmic reticulum mitochondria encounter structure (ERMES), which tethers the ER to mitochondria and associates with the SAM complex. In here, we provide evidence that Mdm10 phylogenetically belongs to the VDAC/Tom40 superfamily. Contrary to Tom40 and VDAC, Mdm10 exposes long loops towards both sides of the membrane. Analyses of single loop deletion mutants of Mdm10 in the yeast Saccharomyces cerevisiae reveal that the loops are dispensable for Mdm10 function. Sequences similar to fungal Mdm10 can be found in species from Excavates to Fungi, but neither in Metazoa nor in plants. Strikingly, the presence of Mdm10 coincides with the appearance of the other ERMES components. Mdm10's presence in both unikonts and bikonts indicates an introduction at an early time point in eukaryotic evolution.     

Homonuclear and heteronuclear transition metal complexes by syn-proportionation reactions

Redox processes consisting of disproportionation and syn-proportionation are reviewed with special attention to metal complexes containing carbon-based ligands, i.e. carbon monoxide or unsaturated hydrocarbons. An introduction and a survey of reactions aimed to show the large applicability of syn-proportionation reactions in the field of coordination chemistry, is followed by examples of the use of these redox processes for the preparation of catalytic precursors. The latter studies derive from the idea that if a syn-proportionation reaction can be carried out between two complexes containing different metals in different oxidation states, inter-metallic systems could be formed which may act as active catalysts, e.g. for polymerization reactions.     

Distinct requirement for an intact dimer interface in wild-type, V600E and kinase-dead B-Raf signalling

The dimerisation of Raf kinases involves a central cluster within the kinase domain, the dimer interface (DIF). Yet, the importance of the DIF for the signalling potential of wild-type B-Raf (B-Raf(wt)) and its oncogenic counterparts remains unknown. Here, we show that the DIF plays a pivotal role for the activity of B-Raf(wt) and several of its gain-of-function (g-o-f) mutants. In contrast, the B-Raf(V600E), B-Raf(insT) and B-Raf(G469A) oncoproteins are remarkably resistant to mutations in the DIF. However, compared with B-Raf(wt), B-Raf(V600E) displays extended protomer contacts, increased homodimerisation and incorporation into larger protein complexes. In contrast, B-Raf(wt) and Raf-1(wt) mediated signalling triggered by oncogenic Ras as well as the paradoxical activation of Raf-1 by kinase-inactivated B-Raf require an intact DIF. Surprisingly, the B-Raf DIF is not required for dimerisation between Raf-1 and B-Raf, which was inactivated by the D594A mutation, sorafenib or PLX4720. This suggests that paradoxical MEK/ERK activation represents a two-step mechanism consisting of dimerisation and DIF-dependent transactivation. Our data further implicate the Raf DIF as a potential target against Ras-driven Raf-mediated (paradoxical) ERK activation.