With the rapid development of nanotechnology in the recent decade, novel DNA and RNA delivery systems for gene therapy have become available that can be used instead of viral vectors. These non-viral vectors can be made of a variety of materials, including inorganic nanoparticles, carbon nanotubes, liposomes, protein and peptide-based nanoparticles, as well as nanoscale polymeric materials. They have as advantages over viral vectors a decreased immune response, and additionally offer flexibility in design, allowing them to be functionalized and targeted to specific sites in a biological system with low cytotoxicity. The focus of this review is to provide an overview of novel nanotechnology-based methods to deliver DNA and small interfering RNAs into biological systems.

Summary: Successful modification of plant cell‐wall composition without compromising plant integrity is dependent on being able to modify the expression of specific genes, but this can be very challenging when the target genes are members of multigene families. 4‐coumarate:CoA ligase (4CL) catalyzes the formation of 4‐coumaroyl CoA, a precursor of both flavonoids and monolignols, and is an attractive target for transgenic down‐regulation aimed at improving agro‐industrial properties. Inconsistent phenotypes of transgenic plants have been attributed to variable levels of down‐regulation of multiple 4CL genes. Phylogenetic analysis of the sorghum genome revealed 24 4CL(‐like) proteins, five of which cluster with bona fide 4CLs from other species. Using a map‐based cloning approach and analysis of two independent mutant alleles, the sorghum brown midrib2 (bmr2) locus was shown to encode 4CL. In vitro enzyme assays indicated that its preferred substrate is 4‐coumarate. Missense mutations in the two bmr2 alleles result in loss of 4CL activity, probably as a result of improper folding as indicated by molecular modeling. Bmr2 is the most highly expressed 4CL in sorghum stems, leaves and roots, both at the seedling stage and in pre‐flowering plants, but the products of several paralogs also display 4CL activity and compensate for some of the lost activity. The contribution of the paralogs varies between developmental stages and tissues. Gene expression assays indicated that Bmr2 is under auto‐regulatory control, as reduced 4CL activity results in over‐expression of the defective gene. Several 4CL paralogs are also up‐regulated in response to the mutation.

With the advent of biorefinery technologies enabling plant biomass to be processed into biofuel, many researchers set out to study and improve candidate biomass crops. Many of these candidates are C4 grasses, characterized by a high productivity and resource use efficiency. In this review the potential of five C4 grasses as lignocellulose feedstock for biofuel production is discussed. These include three important field crops - maize, sugarcane and sorghum - and two undomesticated perennial energy grasses - miscanthus and switchgrass. Although all these grasses are high yielding, they produce different products. While miscanthus and switchgrass are exploited exclusively for lignocellulosic biomass, maize, sorghum and sugarcane are dual-purpose crops. It is unlikely that all the prerequisites for the sustainable and economic production of biomass for a global cellulosic biofuel industry will be fulfilled by a single crop. High and stable yields of lignocellulose are required in diverse environments worldwide, to sustain a year-round production of biofuel. A high resource use efficiency is indispensable to allow cultivation with minimal inputs of nutrients and water and the exploitation of marginal soils for biomass production. Finally, the lignocellulose composition of the feedstock should be optimized to allow its efficient conversion into biofuel and other by-products. Breeding for these objectives should encompass diverse crops, to meet the demands of local biorefineries and provide adaptability to different environments. Collectively, these C4 grasses are likely to play a central role in the supply of lignocellulose for the cellulosic ethanol industry. Moreover, as these species are evolutionary closely related, advances in each of these crops will expedite improvements in the other crops. This review aims to provide an overview of their potential, prospects and research needs as lignocellulose feedstocks for the commercial production of biofuel.

Lignin is an aromatic polymer that makes up 15–30% of the cell walls of terrestrial plants. While lignin's role in facilitating water transport through the vasculature, providing rigidity and acting as a defense against pests and pathogens is important for the plant's survival, industries that process plant biomass for the production of biofuels and bio‐based chemicals have historically primarily been interested in the cell wall polysaccharides, especially cellulose. Consequently, lignin is generated in large quantities as a by‐product that is often burned to generate heat and electricity, or that is used in low‐value applications. It is becoming clear that, rather than treating it as waste, lignin is very suitable for the production of enhanced composites, carbon fibers, and nanomaterials, which offers both economic and environmental benefits. This review highlights recent uses of these polymers as adsorbents, flocculants, adhesives, anti‐oxidants, energy storing films, and vehicles for drug delivery and gene therapy. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci.2015,132, 42069.