Malolactic Fermentation: The ABC’s of MLF

There are two main fermentations associated with the winemaking process. Alcoholic fermentation is conducted bythe yeast culture and malolactic fermentation takes place as a result of the metabolic activity of lactic acid bacteria,specifically from the genera Oenococcus, Lactobacillus, Pediococcus and Leuconostoc. Malolactic fermentation isdefined as the conversion of malic acid to lactic acid and CO2 and besides deacidification also contributes to microbialstability and modification of the aroma profile. This paper aims to provide a comprehensive review discussing all themain aspects and factors related to malolactic fermentation, including practical considerations for monitoring andensuring a successful fermentation

Fast Dynamic Color Switching in Temperature-Responsive Plasmonic Films

This research was supported by UK Engineering and Physical Sciences Research Council grants EP/G060649/1 and EP/L027151/1, and ERC grant LINASS 320503. F.B. thanks the supports from the Winton Programme for the Physics of Sustainability.This is the final version of the article. It first appeared from Wiley via https://doi.org/10.1002/adom.20160009

Plant diversity in secondary, montane grasslands – a case study of the abandoned plantations of Mariepskop Mountain, South Africa

Grasslands are one of the most threatened terrestrial ecosystem types, and montane grasslands of particular conservation concern. Despite high rates of transformation in recent decades, croplands and plantations are being abandoned in parts of many countries, creating an opportunity for conservation of montane grasslands through restoration. We report on the changes in the cover of major vegetation types (indigenous forest, grassland, and plantations) between 1935 and 2022, in an area that was intensively afforested from 1930 to 1960 and abandoned in 2000. Montane grassland at the site declined from over 50% of all landcover to below 15%, but subsequently recovered to 30% within 20 years. Many former plantations developed into secondary grassland with estimated gamma plant species richness of 231 for herbaceous species and 45 for savanna species. These are high values considering the size of the study area (4000 ha), and comparable to estimates from primary grassland sites in the broader region. However, at the scale of 1 m2 sampling quadrats, richness in the secondary grasslands was below that recorded in the last remaining patches of primary grassland at the site (means of 2.6 versus 4.7 for graminoid species, and 1.9 versus 2.9 for forbs). Some of the former Eucalyptus plantations had transformed into novel savannas dominated by fire-tolerant, resprouting trees, and may require more active restoration. Secondary grasslands such as those reported on here could potentially make a significant contribution to the conservation of montane biodiversity over the coming decades, warranting further research (both socio-economic and ecological) on the factors that lead to abandonment and promote the emerge of secondary grasslands of high diversity

Весовые соотношения тимуса и надпочечников у антенатально погибших плодов

ТИМУСНАДПОЧЕЧНИКИтимомегалиядети первого года жизнидети раннего возрастаМЛАДЕНЕЦ, СМЕРТНОСТЬЭНДОКРИННОЙ СИСТЕМЫ БОЛЕЗНИСМЕРТНОСТЬ ДЕТСКАЯсиндром внезапной детской смерт

Human Macrophages Infected with a High Burden of ESAT-6-Expressing M. tuberculosis Undergo Caspase-1- and Cathepsin B-Independent Necrosis

Mycobacterium tuberculosis (Mtb) infects lung macrophages, which instead of killing the pathogen can be manipulated by the bacilli, creating an environment suitable for intracellular replication and spread to adjacent cells. The role of host cell death during Mtb infection is debated because the bacilli have been shown to be both anti-apoptotic, keeping the host cell alive to avoid the antimicrobial effects of apoptosis, and pro-necrotic, killing the host macrophage to allow infection of neighboring cells. Since mycobacteria activate the NLRP3 inflammasome in macrophages, we investigated whether Mtb could induce one of the recently described inflammasome-linked cell death modes pyroptosis and pyronecrosis. These are mediated through caspase-1 and cathepsin-B, respectively. Human monocyte-derived macrophages were infected with virulent (H37Rv) Mtb at a multiplicity of infection (MOI) of 1 or 10. The higher MOI resulted in strongly enhanced release of IL-1β, while a low MOI gave no IL-1β response. The infected macrophages were collected and cell viability in terms of the integrity of DNA, mitochondria and the plasma membrane was determined. We found that infection with H37Rv at MOI 10, but not MOI 1, over two days led to extensive DNA fragmentation, loss of mitochondrial membrane potential, loss of plasma membrane integrity, and HMGB1 release. Although we observed plasma membrane permeabilization and IL-1β release from infected cells, the cell death induced by Mtb was not dependent on caspase-1 or cathepsin B. It was, however, dependent on mycobacterial expression of ESAT-6. We conclude that as virulent Mtb reaches a threshold number of bacilli inside the human macrophage, ESAT-6-dependent necrosis occurs, activating caspase-1 in the process

TRIM27 Negatively Regulates NOD2 by Ubiquitination and Proteasomal Degradation

NOD2, the nucleotide-binding domain and leucine-rich repeat containing gene family (NLR) member 2 is involved in mediating antimicrobial responses. Dysfunctional NOD2 activity can lead to severe inflammatory disorders, but the regulation of NOD2 is still poorly understood. Recently, proteins of the tripartite motif (TRIM) protein family have emerged as regulators of innate immune responses by acting as E3 ubiquitin ligases. We identified TRIM27 as a new specific binding partner for NOD2. We show that NOD2 physically interacts with TRIM27 via the nucleotide-binding domain, and that NOD2 activation enhances this interaction. Dependent on functional TRIM27, ectopically expressed NOD2 is ubiquitinated with K48-linked ubiquitin chains followed by proteasomal degradation. Accordingly, TRIM27 affects NOD2-mediated pro-inflammatory responses. NOD2 mutations are linked to susceptibility to Crohns disease. We found that TRIM27 expression is increased in Crohns disease patients, underscoring a physiological role of TRIM27 in regulating NOD2 signaling. In HeLa cells, TRIM27 is partially localized in the nucleus. We revealed that ectopically expressed NOD2 can shuttle to the nucleus in a Walker A dependent manner, suggesting that NOD2 and TRIM27 might functionally cooperate in the nucleus. We conclude that TRIM27 negatively regulates NOD2-mediated signaling by degradation of NOD2 and suggest that TRIM27 could be a new target for therapeutic intervention in NOD2-associated diseases.Funding Agencies|German Research Foundation (DFG)|SFB670-NG01|Swedish Society of Medicine||Regional Research Council of South-East Sweden (FORSS)||Swedish Research Council division of Medicine||Gustav V 90th anniversary foundation||Italian Telethon Foundation||DFG|SE 1122/2-1|</p