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1.
Sci Rep ; 12(1): 2445, 2022 02 14.
Article in English | MEDLINE | ID: mdl-35165351

ABSTRACT

Surgical masks have become critical for protecting human health against the COVID-19 pandemic, even though their environmental burden is a matter of ongoing debate. This study aimed at shedding light on the environmental impacts of single-use (i.e., MD-Type I) versus reusable (i.e., MD-Type IIR) face masks via a comparative life cycle assessment with a cradle-to-grave system boundary. We adopted a two-level analysis using the ReCiPe (H) method, considering both midpoint and endpoint categories. The results showed that reusable face masks created fewer impacts for most midpoint categories. At the endpoint level, reusable face masks were superior to single-use masks, producing scores of 16.16 and 84.20 MPt, respectively. The main environmental impacts of single-use masks were linked to raw material consumption, energy requirements and waste disposal, while the use phase and raw material consumption made the most significant contribution for reusable type. However, our results showed that lower environmental impacts of reusable face masks strongly depend on the use phase since reusable face masks lost their superior performance when the hand wash scenario was tested. Improvement of mask eco-design emerged as another key factor such as using more sustainable raw materials and designing better waste disposal scenarios could significantly lower the environmental impacts.


Subject(s)
COVID-19/prevention & control , Masks/standards , Personal Protective Equipment/standards , Textiles/standards , COVID-19/epidemiology , COVID-19/virology , Disposable Equipment/standards , Ecosystem , Environment , Equipment Reuse/standards , Humans , Masks/classification , Pandemics/prevention & control , Personal Protective Equipment/classification , Public Health/methods , SARS-CoV-2/physiology , Textiles/classification
2.
J Biosci Bioeng ; 114(1): 45-52, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22575437

ABSTRACT

In the present study, osmoadaptive mechanism of Halomonas sp. AAD12 was studied through analysis of changes in its proteome maps and osmolyte accumulation strategy to understand how this euryhaline microorganism masters osmotic stress of saline environments. Under salt stress, there were significant variations in the expression of proteins involved in osmoregulation, stress response, energy generation and transport. This was accompanied by an increase in proline and hydroxyectoine but a decrease in ectoine accumulation. The major osmolyte at high salinity was proline. Unexpectedly the size of the total ectoines' pool was smaller at elevated salinity. Experimental findings were then integrated with a metabolic model to get insight into carbon trafficking during osmoadaptation. Simulations predicted that the total flux through energy generating pathways, namely gluconeogenesis and the pentose phosphate pathway, was significantly lower and carbon source that entered the system as citrate was mainly diverted to osmolyte synthesis at high salinity. Overall these results suggested that the moderately halophilic Halomonas sp. AAD12 pursued a different osmoregulatory strategy than the two well known moderate halophiles, Chromohalobacter salexigens and Halobacillus halophilus. The climbing value of osmolytes such as ectoine in health care and skin care products places significant attention to halophilic microorganisms hence an understanding of the osmoadaptive mechanism and osmolyte accumulation strategy of this isolate is very valuable to be able to manipulate its metabolism towards desired goals.


Subject(s)
Adaptation, Physiological/physiology , Halomonas/physiology , Stress, Physiological , Adaptation, Physiological/drug effects , Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Biological Transport , Computer Simulation , Gene Expression Regulation, Bacterial , Halomonas/drug effects , Halomonas/metabolism , Molecular Sequence Data , Proteome , Salinity , Sodium Chloride/pharmacology , Stress, Physiological/drug effects
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