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However, to our knowledge, only one study has reported growth promotion of a bioenergy feedstock grass (Miscanthus x giganteous) seedlings by a bacterial endophyte (Herbaspirillum frisingense) [ 18].
Methods that combine MALDI and SIMS imaging have been utilized recently for multiscale chemical mapping of nervous tissue, skin and kidney, single cultured neurons, bacterial biofilms, and a biofuel feedstock grass.
Li et al. correlated CRM, SIMS, and laser desorption ionization (LDI) MSI to elucidate the subcellular localization of carbohydrates (cellulose and hemicellulose) in biofuel feedstock grass, allowing more definitive mass and vibrational assignments from mutually observed chemical features.
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Framed upon the 2009 sorghum reference genome [ 7], translational genomic resources have been developed that directly impact research in other closely related C4 feedstock grasses, including switchgrass and Miscanthus[ 8, 9].
(slender false-brome; Poaceae), with an estimated genome size of 470 Mb and 17 chromosomes (Foote et al., 2004), is a perennial bunchgrass native to Europe, Asia, and North Africa and is closely related to the bioenergy feedstock model grass B. distachyon (L).
Feedstock includes grasses and bamboos as well as timber.
The bioenergy grass feedstock traits that underlie conversion efficiency are being elucidated opening the door to genetic enhancement from existing feedstock.
Grass crop supply chains may also include densification, drying, and other forms of preprocessing as well as pretreatments that chemically alter grass feedstock.
Despite its ecological advantages compared to maize, an enlargement of the share of grass feedstock is not assumed here because permanent grassland is less competitive in many regions compared to cropping systems [55].
First, bioenergy grass feedstock traits relevant to biochemical conversion are examined.
There are many extant bioenergy grass feedstock varieties (genotypes), which are sufficient for select conversion processes.
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