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Environmental impacts and consumer concerns have necessitated the study of bio-based materials as alternatives to petrochemicals for packaging applications. The purpose of this review is to summarize synthetic and non-synthetic materials feasible for packaging and textile applications, routes of upscaling, (industrial) applications, evaluation of sustainability, and end-of-life options. The outlined bio-based materials include polylactic acid, polyethylene furanoate, polybutylene succinate, and non-synthetically produced polymers such as polyhydrodyalkanoate, cellulose, starch, proteins, lipids, and waxes. Further emphasis is placed on modification techniques (coating and surface modification), biocomposites, multilayers, and additives used to adjust properties especially for barriers to gas and moisture and to tune their biodegradability. Overall, this review provides a holistic view of bio-based packaging material including processing, and an evaluation of the sustainability of and options for recycling. Thus, this review contributes to increasing the knowledge of available sustainable bio-based packaging material and enhancing the transfer of scientific results into applications.

Biobased plastics are fully or partially made from biological resources but are not necessarily biodegradable or compostable. Poly (lactic acid) (PLA), one of the most diffused bioplastics, is compostable in industrial environments, but improving degradation in home composting conditions, in soil and in seawater could be beneficial for improving its end of life and general degradability. Blends obtained by the extrusion of PLA with different amounts of poly (butylene succinate-co-adipate) (PBSA) or poly (caprolactone) (PCL) were characterized in terms of their home composting, soil, marine and freshwater biodegradation. The blending strategy was found to be successful in improving the home compostability and soil compostability of PLA. Thanks to the correlations with morphological characterization as determined by electron microscopy, it was possible to show that attaining an almost co-continuous phase distribution, depending on the composition and melt viscosity of the blend components, can enhance PLA degradation in home composting conditions. Tests in marine and freshwater were also performed, and the obtained results showed that in marine conditions, pure PLA is degradable. A comparison of different tests evidenced that salt dissolved in marine water plays an important role in favoring PLA’s degradability.

Biobased plastics are fully or partially made from biological resources but are not necessarily biodegradable or compostable. Poly (lactic acid) (PLA), one of the most diffused bioplastics, is compostable in industrial environments, but improving degradation in home composting conditions, in soil and in seawater could be beneficial for improving its end of life and general degradability. Blends obtained by the extrusion of PLA with different amounts of poly (butylene succinate-co-adipate) (PBSA) or poly (caprolactone) (PCL) were characterized in terms of their home composting, soil, marine and freshwater biodegradation. The blending strategy was found to be successful in improving the home compostability and soil compostability of PLA. Thanks to the correlations with morphological characterization as determined by electron microscopy, it was possible to show that attaining an almost co-continuous phase distribution, depending on the composition and melt viscosity of the blend components, can enhance PLA degradation in home composting conditions. Tests in marine and freshwater were also performed, and the obtained results showed that in marine conditions, pure PLA is degradable. A comparison of different tests evidenced that salt dissolved in marine water plays an important role in favoring PLA’s degradability.

ARABIDOPSIS THALIANA CYTOCHROME P450 REDUCTASE1 (ATR1) and ATR2 provide electrons from NADPH to a large number of CYTOCHROME P450 (CYP450) enzymes in Arabidopsis (Arabidopsis thaliana). Whereas ATR1 is constirutively expressed, the expression of ATR2 appears to be induced during lignin biosynthesis and upon stresses. Therefore, ATR2 was hypothesized to be preferentially involved in providing electrons to the three CYP450s involved in lignin biosynthesis: CINNAMATE 4-HYDROXYLASE (C4H), p-COUMARATE 3-HYDROXYLASE1 (C3H1), and FERULATE 5-HYDROXYLASE1 (F5H1). Here, we show that the airt mutation resulted in a 6% reduction in total lignin amount in the main inflorescence stem and a compositional shift of the remaining lignin to a 10-fold higher fraction of p-hydroxyphenyl units at the expense of syringyl units. Phenolic profiling revealed shifts in lignin-related phenolic metabolites, in particular with the substrates of C4H, C3H1 and F5H1 accumulating in atr2 mutants. Glucosinolate and flavonol glycoside biosynthesis, both of which also rely on CYP450 activities, appeared less affected. The cellulose in the atr2 inflorescence stems was more susceptible to enzymatic hydrolysis after alkaline pretreatment, making ATR2 a potential target for engineering plant cell walls for biofuel production.