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Dive into the research topics where Brenna A. Black is active.

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Featured researches published by Brenna A. Black.


Bioresource Technology | 2016

Succinic acid production from lignocellulosic hydrolysate by Basfia succiniciproducens

Davinia Salvachúa; Holly Smith; Peter C. St. John; Ali Mohagheghi; Darren J. Peterson; Brenna A. Black; Nancy Dowe; Gregg T. Beckham

The production of chemicals alongside fuels will be essential to enhance the feasibility of lignocellulosic biorefineries. Succinic acid (SA), a naturally occurring C4-diacid, is a primary intermediate of the tricarboxylic acid cycle and a promising building block chemical that has received significant industrial attention. Basfia succiniciproducens is a relatively unexplored SA-producing bacterium with advantageous features such as broad substrate utilization, genetic tractability, and facultative anaerobic metabolism. Here B. succiniciproducens is evaluated in high xylose-content hydrolysates from corn stover and different synthetic media in batch fermentation. SA titers in hydrolysate at an initial sugar concentration of 60g/L reached up to 30g/L, with metabolic yields of 0.69g/g, and an overall productivity of 0.43g/L/h. These results demonstrate that B. succiniciproducens may be an attractive platform organism for bio-SA production from biomass hydrolysates.


Green Chemistry | 2016

Lignin depolymerization by fungal secretomes and a microbial sink

Davinia Salvachúa; Rui Katahira; Nicholas S. Cleveland; Payal Khanna; Michael G. Resch; Brenna A. Black; Samuel O. Purvine; Erika Zink; Alicia Prieto; María Jesús Martínez; Ángel T. Martínez; Blake A. Simmons; John M. Gladden; Gregg T. Beckham

In Nature, powerful oxidative enzymes secreted by white rot fungi and some bacteria catalyze lignin depolymerization and some microbes are able to catabolize the resulting aromatic compounds as carbon and energy sources. Taken together, these two processes offer a potential route for microbial valorization of lignin. However, many challenges remain in realizing this concept, including that oxidative enzymes responsible for lignin depolymerization also catalyze polymerization of low molecular weight (LMW) lignin. Here, multiple basidiomycete secretomes were screened for ligninolytic enzyme activities in the presence of a residual lignin solid stream from a corn stover biorefinery, dubbed DMR-EH (Deacetylation, Mechanical Refining, and Enzymatic Hydrolysis) lignin. Two selected fungal secretomes, with high levels of laccases and peroxidases, were utilized for DMR-EH lignin depolymerization assays. The secretome from Pleurotus eryngii, which exhibited the highest laccase activity, reduced the lignin average molecular weight (Mw) by 63% and 75% at pH 7 compared to the Mw of the control treated at the same conditions and the initial DMR-EH lignin, respectively, and was applied in further depolymerization assays as a function of time. As repolymerization was observed after 3 days of incubation, an aromatic-catabolic microbe (Pseudomonas putida KT2440) was incubated with the fungal secretome and DMR-EH lignin. These experiments demonstrated that the presence of the bacterium enhances lignin depolymerization, likely due to bacterial catabolism of LMW lignin, which may partially prevent repolymerization. In addition, proteomics was also applied to the P. eryngii secretome to identify the enzymes present in the fungal cocktail utilized for the depolymerization assays, which highlighted a significant number of glucose/methanol/choline (GMC) oxidoreductases and laccases. Overall, this study demonstrates that ligninolytic enzymes can be used to partially depolymerize a solid, high lignin content biorefinery stream and that the presence of an aromatic-catabolic bacterium as a “microbial sink” improves the extent of enzymatic lignin depolymerization.


Energy and Environmental Science | 2018

Thermochemical wastewater valorization via enhanced microbial toxicity tolerance

Lahiru N. Jayakody; Christopher W. Johnson; Jason M. Whitham; Richard J. Giannone; Brenna A. Black; Nicholas S. Cleveland; Dawn M. Klingeman; William E. Michener; Jessica L. Olstad; Derek R. Vardon; Robert C. Brown; Steven D. Brown; Robert L. Hettich; Adam M. Guss; Gregg T. Beckham

Thermochemical (TC) biomass conversion processes such as pyrolysis and liquefaction generate considerable amounts of wastewater, which often contains highly toxic compounds that are incredibly challenging to convert via standard wastewater treatment approaches such as anaerobic digestion. These streams represent a cost for TC biorefineries, and a potential valorization opportunity, if effective conversion methods are developed. The primary challenge hindering microbial conversion of TC wastewater is toxicity. In this study, we employ a robust bacterium, Pseudomonas putida, with TC wastewater streams to demonstrate that aldehydes are the most inhibitory compounds in these streams. Proteomics, transcriptomics, and fluorescence-based immunoassays of P. putida grown in a representative wastewater stream indicate that stress results from protein damage, which we hypothesize is a primary toxicity mechanism. Constitutive overexpression of the chaperone genes, groEL, groES, and clpB, in a genome-reduced P. putida strain improves the tolerance towards multiple TC wastewater samples up to 200-fold. Moreover, the concentration ranges of TC wastewater are industrially relevant for further bioprocess development for all wastewater streams examined here, representing different TC process configurations. Furthermore, we demonstrate proof-of-concept polyhydroxyalkanoate production from the usable carbon in an exemplary TC wastewater stream. Overall, this study demonstrates that protein quality control machinery and repair mechanisms can enable substantial gains in microbial tolerance to highly toxic substrates, including heterogeneous waste streams. When coupled to other metabolic engineering advances such as expanded substrate utilization and enhanced product accumulation, this study generally enables new strategies for biological conversion of highly-toxic, organic-rich wastewater via engineered aerobic monocultures or designer consortia.


Green Chemistry | 2018

Integrated diesel production from lignocellulosic sugars via oleaginous yeast

Violeta Sànchez i Nogué; Brenna A. Black; Jacob S. Kruger; Christine A. Singer; Kelsey J. Ramirez; Michelle Reed; Nicholas S. Cleveland; Emily R. Singer; Xiunan Yi; Rou Yi Yeap; Jeffrey G. Linger; Gregg T. Beckham

Oleaginous microbes are promising platform strains for the production of renewable diesel and fatty-acid derived chemicals given their innate capacity to produce high lipid yields from lignocellulose-derived sugars. Substantial efforts have been conducted to engineer model oleaginous yeasts primarily on model feedstocks, but to enable lipid production from biomass, judicious strain selection based on phenotypes beneficial for processing, performance on realistic feedstocks, and process integration aspects from sugars to fuels should be examined holistically. To that end, here we report the bench-scale production of diesel blendstock using a biological-catalytic hybrid process based on oleaginous yeast. This work includes flask screening of 31 oleaginous yeast strains, evaluated based on baseline lipid profiles and sugar consumption with corn stover hydrolysate. Three strains were down-selected for bioreactor performance evaluation. The cultivation results reveal that Cryptococcus curvatus ATCC 20509 and Rhodosporodium toruloides DSM-4444 exhibit equivalent fatty acid methyl ester (FAME) yield (0.24 g g−1), whereas the highest overall FAME productivity (0.22 g L−1 h−1) was obtained with C. curvatus, and R. toruloides displayed the highest final FAME titer (23.3 g L−1). Time-resolved lipid profiling (including neutral and polar lipid classing) demonstrated triacylglycerol accumulation as the predominant lipid class in all strains. When evaluating tolerance mechanisms to inhibitory compounds, all strains could reduce and oxidize 5-(hydroxymethyl)furfural, illustrating parallel detoxification mechanisms. The R. toruloides strain was also capable of growth on four aromatic compounds as a sole carbon source, suggesting its use as a strain for simultaneous sugar and lignin conversion. Lipids from R. toruloides were recovered using a mild acid treatment and extraction, hydrogenated, and isomerized to produce a renewable diesel blendstock. The blendstock exhibited a cloud point of −14.5 °C and simulated distillation showed that approximately 75% of the product was in the diesel range with a T90 consistent with no. 2 diesel fuel. Taken together, these results demonstrate an integrated process for renewable diesel production, identify oleaginous strains for further development, and highlight opportunities for improvements to an oleaginous microbial platform for the production of renewable diesel blendstock.


Green Chemistry | 2018

Bioprocess development for muconic acid production from aromatic compounds and lignin

Davinia Salvachúa; Christopher W. Johnson; Christine A. Singer; Holly Rohrer; Darren J. Peterson; Brenna A. Black; Anna Knapp; Gregg T. Beckham

Muconic acid (MA) is a bio-based platform chemical that can be converted into the commodity petrochemical building blocks adipic acid or terephthalic acid, or used in emerging, performance-advantaged materials. MA is a metabolic intermediate in the β-ketoadipate pathway, and can be produced from carbohydrates or other traditional carbon sources via the shikimate pathway. MA can also be produced from lignin-derived aromatic compounds with high atom efficiency through aromatic-catabolic pathways. Metabolic engineering efforts to date have developed efficient muconic acid-producing strains of the aromatic-catabolic microbe Pseudomonas putida KT2440, but the titers, productivities, and yields from aromatic compounds in most cases remain below the thresholds needed for industrially-relevant bioreactor cultivations. To that end, this work presents further process and host development towards improving MA titers, yields, and productivities, using the hydroxycinnamic acids, p-coumaric acid and ferulic acid, as model aromatic compounds. Coupling strain engineering and bioprocess development enabled the discovery of new bottlenecks in P. putida that hinder MA production from these compounds. A combination of gene overexpression and removal of a global catabolic regulator resulted in high-yielding strains (100% molar yield). Maximum MA titers of 50 g L−1, which is near the lethal toxicity limit in this bacterium, and productivities over 0.5 g L−1 h−1 were achieved in separate process configurations. Additionally, a high-pH feeding strategy, which could potentially reduce the salt load and enable higher titers by decreasing product dilution, was tested with model compounds and lignin-rich streams from corn stover and a complete conversion of the primary monomeric aromatic compounds to MA was demonstrated, obtaining a titer of 4 g L−1. Overall, this study presents a step forward for the production of value-added chemicals from lignin and highlights critical needs for further strain improvement and bioprocess development that can be applied in the biological valorization of lignin.


Biotechnology for Biofuels | 2016

Succinic acid production on xylose-enriched biorefinery streams by Actinobacillus succinogenes in batch fermentation

Davinia Salvachúa; Ali Mohagheghi; Holly Smith; Michael F. A. Bradfield; Willie Nicol; Brenna A. Black; Mary J. Biddy; Nancy Dowe; Gregg T. Beckham


Biotechnology for Biofuels | 2015

Continuous Succinic Acid Production by Actinobacillus succinogenes on Xylose-Enriched Hydrolysate

Michael F. A. Bradfield; Ali Mohagheghi; Davinia Salvachúa; Holly Smith; Brenna A. Black; Nancy Dowe; Gregg T. Beckham; Willie Nicol


ACS Catalysis | 2016

Lignin Depolymerization with Nitrate-Intercalated Hydrotalcite Catalysts

Jacob S. Kruger; Nicholas S. Cleveland; Shuting Zhang; Rui Katahira; Brenna A. Black; Gina M. Chupka; Tijs Lammens; Phillip G. Hamilton; Mary J. Biddy; Gregg T. Beckham


ACS Sustainable Chemistry & Engineering | 2017

Base-Catalyzed Depolymerization of Solid Lignin-Rich Streams Enables Microbial Conversion

Alberto Rodriguez; Davinia Salvachúa; Rui Katahira; Brenna A. Black; Nicholas S. Cleveland; Michelle Reed; Holly Smith; Edward E. K. Baidoo; Jay D. Keasling; Blake A. Simmons; Gregg T. Beckham; John M. Gladden


ACS Sustainable Chemistry & Engineering | 2016

Aqueous Stream Characterization from Biomass Fast Pyrolysis and Catalytic Fast Pyrolysis

Brenna A. Black; William E. Michener; Kelsey J. Ramirez; Mary J. Biddy; Brandon C. Knott; Mark W. Jarvis; Jessica L. Olstad; Ofei D. Mante; David C. Dayton; Gregg T. Beckham

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Gregg T. Beckham

National Renewable Energy Laboratory

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Davinia Salvachúa

National Renewable Energy Laboratory

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Nicholas S. Cleveland

National Renewable Energy Laboratory

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Holly Smith

National Renewable Energy Laboratory

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Rui Katahira

University of North Texas

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William E. Michener

National Renewable Energy Laboratory

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Ali Mohagheghi

National Renewable Energy Laboratory

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Mary J. Biddy

National Renewable Energy Laboratory

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Michelle Reed

National Renewable Energy Laboratory

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Nancy Dowe

National Renewable Energy Laboratory

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