CHAPTER 5. Advances in the Genetic Manipulation of Cellulosic Bioenergy Crops for Bioethanol Production

Author(s):  
Chuansheng Mei ◽  
Callista Rakhmatov
Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3870
Author(s):  
Jingyang Li ◽  
Fei Liu ◽  
Hua Yu ◽  
Yuqi Li ◽  
Shiguang Zhou ◽  
...  

Banana is a major fruit crop throughout the world with abundant lignocellulose in the pseudostem and rachis residues for biofuel production. In this study, we collected a total of 11 pseudostems and rachis samples that were originally derived from different genetic types and ecological locations of banana crops and then examined largely varied edible carbohydrates (soluble sugars, starch) and lignocellulose compositions. By performing chemical (H2SO4, NaOH) and liquid hot water (LHW) pretreatments, we also found a remarkable variation in biomass enzymatic saccharification and bioethanol production among all banana samples examined. Consequently, this study identified a desirable banana (Refen1, subgroup Pisang Awak) crop containing large amounts of edible carbohydrates and completely digestible lignocellulose, which could be combined to achieve the highest bioethanol yields of 31–38% (% dry matter), compared with previously reported ones in other bioenergy crops. Chemical analysis further indicated that the cellulose CrI and lignin G-monomer should be two major recalcitrant factors affecting biomass enzymatic saccharification in banana pseudostems and rachis. Therefore, this study not only examined rich edible carbohydrates for food in the banana pseudostems but also detected digestible lignocellulose for bioethanol production in rachis tissue, providing a strategy applicable for genetic breeding and biomass processing in banana crops.


2021 ◽  
Vol 29 ◽  
pp. 13-19
Author(s):  
R. Y. Blume ◽  
O.V. Melnychuk ◽  
S.P. Ozheredov ◽  
D.B. Rakhmetov ◽  
Y.B. Blume

Aim. Main aim of this research was the evaluation of theoretical bioethanol yield (per ha) from hexaploid giant miscanthus (Miscanthus х giganteus) and further comparison with conventional triploid form as well as with other bioethanol crops. Methods. Several mathematic functions were determined that describe yearly yield dynamics and equations, which were used in calculations of theoretical bioethanol yield. Results. The theoretical bioethanol yield was evaluated for different hexaploid miscanthus lines. The most productive in terms of ethanol yield were lines 108 and 202, from which potential bioethanol yield was found to be higher than in control line (6451 L/ha) by 10.7 % and 14.2% respectively and can reach 7144 L/ha and 7684 L/ha. Conclusions. It was determined that the most productive lines of polyploid miscanthus (lines 108 and 202) are able to compete with other plant cellulosic feedstocks for second-generation bioethanol production in Ukraine. However, these lines show bioethanol productivity than sweet sorghum, in the case when sweet sorghum is processed for obtainment of both first- and second-generation bioethanol. Keywords: bioenergy crops, biofuels, giant miscanthus, Miscanthus, polyploidy, second-generation bioethanol.


2020 ◽  
Vol 75 (1) ◽  
pp. 29-41
Author(s):  
ROMAN MOLAS ◽  
HALINA BORKOWSKA ◽  
DOMINIKA SKIBA ◽  
ALEKSANDRA GŁOWACKA

Through the six successive years (2010–2015), from the 5th to the 10th year of cultivation, research was carried out on yielding and species characteristics of 4 perennial vegetatively propagated energy crops. These were: 2 species of Miscanthus, Sida hermaphrodita, and 2 Salix viminalis clones (1047 and 1054), cultivated side-by-side. The height and shoot number, yield and biomass moisture were evaluated. The highest shoot density of Miscanthus sacchariflorus was found, while the largest yield of Miscanthus × giganteus. Salix viminalis and Miscanthus × giganteus biomass was characterized by the highest content of accumulated moisture (on average 50%). The Sida hermaphrodita plants were appeared as the tallest ones on the six-year average. It is worth mentioning, we have concluded that yield of Miscanthus, and Sida is high and stable in the long-term study. However, in the average yields of these 2 species (Miscanthus × giganteus and Sida hermaphrodita) no statistically significant differences were found. Results can strengthen the improved species diversity in perennial energy crops cultivation.


2018 ◽  
Vol 2 (3) ◽  
pp. 433-442 ◽  
Author(s):  
Qiong Wang ◽  
Michael J. Betenbaugh

As a complex and common post-translational modification, N-linked glycosylation affects a recombinant glycoprotein's biological activity and efficacy. For example, the α1,6-fucosylation significantly affects antibody-dependent cellular cytotoxicity and α2,6-sialylation is critical for antibody anti-inflammatory activity. Terminal sialylation is important for a glycoprotein's circulatory half-life. Chinese hamster ovary (CHO) cells are currently the predominant recombinant protein production platform, and, in this review, the characteristics of CHO glycosylation are summarized. Moreover, recent and current metabolic engineering strategies for tailoring glycoprotein fucosylation and sialylation in CHO cells, intensely investigated in the past decades, are described. One approach for reducing α1,6-fucosylation is through inhibiting fucosyltransferase (FUT8) expression by knockdown and knockout methods. Another approach to modulate fucosylation is through inhibition of multiple genes in the fucosylation biosynthesis pathway or through chemical inhibitors. To modulate antibody sialylation of the fragment crystallizable region, expressions of sialyltransferase and galactotransferase individually or together with amino acid mutations can affect antibody glycoforms and further influence antibody effector functions. The inhibition of sialidase expression and chemical supplementations are also effective and complementary approaches to improve the sialylation levels on recombinant glycoproteins. The engineering of CHO cells or protein sequence to control glycoforms to produce more homogenous glycans is an emerging topic. For modulating the glycosylation metabolic pathways, the interplay of multiple glyco-gene knockouts and knockins and the combination of multiple approaches, including genetic manipulation, protein engineering and chemical supplementation, are detailed in order to achieve specific glycan profiles on recombinant glycoproteins for superior biological function and effectiveness.


2016 ◽  
Vol 2 (1) ◽  
pp. 57-59
Author(s):  
Pavithra D ◽  
Praveen D ◽  
Vijey Aanandhi M

Agranulocytosis is also known to be granulopenia, causing neutropenia in circulating blood streams .The destruction of white blood cells takes place which leads to increase in the infection rate in an individual where immune system of the individual is suppressed. The symptoms includes fever, sore throat, mouth ulcers. These are commonly seen as adverse effects of a particular drug and are prescribed for the common diagnostic test for regular monitoring of complete blood count in an admitted patient. Drug-induced agranulocytosis remains a serious adverse event due to occurrence of severe sepsis with deep infection leading to pneumonia, septicaemia, and septic shock in two/third of the patient. Antibiotics seem to be the major causative weapon for this disorder. Certain drugs mainly anti-thyroid drugs, ticlopidine hydrochloride, spironolactone, clozapine, antileptic drugs (clozapine), non-steroidal anti-inflammatory agents, dipyrone are the potential causes. Bone marrow insufficiency followed by destruction or limited proliferative bone marrow destruction takes place. Chemotherapy is rarely seen as a causative agent for this disorder. Genetic manipulation may also include as one of the reason. Agranulocytosis can be recovered within two weeks but the mortality and morbidity rate during the acute phase seems to be high, appropriate adjuvant treatment with broad-spectrum antibiotics are prerequisites for the management of complicated neutropenia. Drugs that are treated for this are expected to change as a resistant drug to the patient. The pathogenesis of agranulocytosis is not yet known. A comprehensive literature search has been carried out in PubMed, Google Scholar and articles pertaining to drug-induced agranulocytosis were selected for review.


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