Metabolic engineering strategies to enable microbial utilization of C1 feedstocks

Production of first and second generation biofuels: A comprehensive review

Naik, S. N., Goud, V. V., Rout, P. K., & Dalai, A. K. (2010) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2009.10.003 · Cited by 3,264 · see citing works

Acetogenesis and the Wood–Ljungdahl pathway of CO2 fixation

Ragsdale, S. W., & Pierce, E. (2008) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2008.08.012 · Cited by 1,337 · see citing works

Carbon Monoxide Poisoning

Ernst, A., & Zibrak, J. D. (1998) · New England Journal of Medicine · doi:10.1056/nejm199811263392206 · Cited by 1,105 · see citing works

Methanotrophs and copper

Semrau, J. D., DiSpirito, A. A., & Yoon, S. (2010) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2010.00212.x · Cited by 775 · see citing works

Alternative Pathways of Carbon Dioxide Fixation: Insights into the Early Evolution of Life?

Fuchs, G. (2011) · Annual Review of Microbiology · doi:10.1146/annurev-micro-090110-102801 · Cited by 726 · see citing works

Plasmon induced thermoelectric effect in graphene

Shautsova, V., Sidiropoulos, T., Xiao, X., Güsken, N. A., Black, N. C. G., Gilbertson, A. M., Giannini, V., Maier, S. A., Cohen, L. F., & Oulton, R. F. (2018) · Nature Communications · doi:10.1038/s41467-018-07508-z · Cited by 710 · see citing works

A synthetic pathway for the fixation of carbon dioxide in vitro

Schwander, T., von Borzyskowski, L. S., Burgener, S., Cortina, N. S., & Erb, T. J. (2016) · Science · doi:10.1126/science.aah5237 · Cited by 696 · see citing works

Structure, Function, and Mechanism of the Nickel Metalloenzymes, CO Dehydrogenase, and Acetyl-CoA Synthase

Can, M., Armstrong, F. A., & Ragsdale, S. W. (2014) · Chemical Reviews · doi:10.1021/cr400461p · Cited by 625 · see citing works

Synthetic Biology Tools to Engineer Microbial Communities for Biotechnology

McCarty, N. S., & Ledesma‐Amaro, R. (2018) · Trends in biotechnology · doi:10.1016/j.tibtech.2018.11.002 · Cited by 585 · see citing works

Structure and function of Rubisco

Andersson, I., & Backlund, A. (2008) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2008.01.001 · Cited by 563 · see citing works

The emergence of adaptive laboratory evolution as an efficient tool for biological discovery and industrial biotechnology

Sandberg, T. E., Salazar, M. J., Weng, L. L., Palsson, B. Ø., & Feist, A. M. (2019) · Metabolic Engineering · doi:10.1016/j.ymben.2019.08.004 · Cited by 558 · see citing works

Industrial biomanufacturing: The future of chemical production

Clomburg, J. M., Crumbley, A. M., & González, R. (2017) · Science · doi:10.1126/science.aag0804 · Cited by 555 · see citing works

Oxidation of methane by a biological dicopper centre

Balasubramanian, R., Smith, S. M., Rawat, S., Yatsunyk, L. A., Stemmler, T. L., & Rosenzweig, A. C. (2010) · Nature · doi:10.1038/nature08992 · Cited by 546 · see citing works

Conversion of Escherichia coli to Generate All Biomass Carbon from CO2

Gleizer, S., Ben-Nissan, R., Bar‐On, Y. M., Antonovsky, N., Noor, Ε., Zohar, Y., Jona, G., Krieger, E., Shamshoum, M., Bar‐Even, A., et al. (2019) · Cell · doi:10.1016/j.cell.2019.11.009 · Cited by 528 · see citing works

Design and analysis of synthetic carbon fixation pathways

Bar‐Even, A., Noor, Ε., Lewis, N. E., & Milo, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907176107 · Cited by 509 · see citing works

Methane as a Resource: Can the Methanotrophs Add Value?

Strong, P. J., Xie, S., & Clarke, W. P. (2015) · Environmental Science & Technology · doi:10.1021/es504242n · Cited by 501 · see citing works

The Calvin cycle revisited

Raines, C. A. (2003) · Photosynthesis Research · doi:10.1023/a:1022421515027 · Cited by 494 · see citing works

Gas Fermentation—A Flexible Platform for Commercial Scale Production of Low-Carbon-Fuels and Chemicals from Waste and Renewable Feedstocks

Liew, F., Martin, M. E., Tappel, R. C., Heijstra, B. D., Mihalcea, C., & Köpke, M. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00694 · Cited by 485 · see citing works

Third-generation biorefineries as the means to produce fuels and chemicals from CO2

Liu, Z., Wang, K., Chen, Y., Tan, T., & Nielsen, J. (2020) · Nature Catalysis · doi:10.1038/s41929-019-0421-5 · Cited by 475 · see citing works

Methanol: The Basic Chemical and Energy Feedstock of the Future

Bertau, M., Offermanns, H., Plass, L., Schmidt, F. K., & Wernicke, H. (2014) · Springer eBooks · doi:10.1007/978-3-642-39709-7 · Cited by 455 · see citing works

Distribution, diversity and ecology of aerobic CO-oxidizing bacteria

King, G. M., & Weber, C. F. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1595 · Cited by 436 · see citing works

PQQ-dependent methanol dehydrogenases: rare-earth elements make a difference

Keltjens, J. T., Pol, A., Reimann, J., & den Camp, H. J. M. O. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-5766-8 · Cited by 415 · see citing works

Computational protein design enables a novel one-carbon assimilation pathway

Siegel, J. B., Smith, A. L., Poust, S. K., Wargacki, A. J., Bar‐Even, A., Louw, C., Shen, B. W., Eiben, C. B., Tran, H. M., Noor, Ε., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1500545112 · Cited by 409 · see citing works

Growth of E. coli on formate and methanol via the reductive glycine pathway

Kim, S., Lindner, S. N., Aslan, S., Yishai, O., Wenk, S., Schann, K., & Bar‐Even, A. (2020) · Nature Chemical Biology · doi:10.1038/s41589-020-0473-5 · Cited by 383 · see citing works

Sugar Synthesis from CO2 in Escherichia coli

Antonovsky, N., Gleizer, S., Noor, Ε., Zohar, Y., Herz, E., Barenholz, U., Zelcbuch, L., Amram, S., Wides, A., Tepper, N., et al. (2016) · Cell · doi:10.1016/j.cell.2016.05.064 · Cited by 369 · see citing works

Renewable methanol and formate as microbial feedstocks

Cotton, C. A. R., Claassens, N. J., Benito-Vaquerizo, S., & Bar‐Even, A. (2019) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2019.10.002 · Cited by 363 · see citing works

The structure of the yeast ribosomal RNA genes. I. The complete nucleotide sequence of the 18S ribosomal RNA gene from Saccharomyces cerevisiae

Rubtsov, P. M., Musakhanov, M. M., Zakharyev, V. M., et al. (1980) · Nucleic Acids Research · doi:10.1093/nar/8.23.5779 · Cited by 347 · see citing works

The formate bio-economy

Yishai, O., Lindner, S. N., de la Cruz, J. G., Tenenboim, H., & Bar‐Even, A. (2016) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2016.07.005 · Cited by 321 · see citing works

The industrial yeast Pichia pastoris is converted from a heterotroph into an autotroph capable of growth on CO2

Gassler, T., Sauer, M., Gasser, B., Egermeier, M., Troyer, C., Causon, T. J., Hann, S., Mattanovich, D., & Steiger, M. G. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0363-0 · Cited by 319 · see citing works

Functional Characterization of the Two Alcohol Oxidase Genes from the Yeast Pichia pastoris

Cregg, J. M., Madden, K. R., Barringer, K., Thill, G. P., & Stillman, C. A. (1989) · Molecular and Cellular Biology · doi:10.1128/mcb.9.3.1316-1323.1989 · Cited by 313 · see citing works

Adaptive laboratory evolution — harnessing the power of biology for metabolic engineering

Portnoy, V. A., Bezdan, D., & Zengler, K. (2011) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2011.03.007 · Cited by 309 · see citing works

The reductive glycine pathway allows autotrophic growth of Desulfovibrio desulfuricans

Sánchez-Andrea, I., Guedes, I. A., Hornung, B., Boeren, S., Lawson, C. E., Sousa, D. Z., Bar-Even, A., Claassens, N. J., & Stams, A. J. M. (2020) · Nature Communications · doi:10.1038/s41467-020-18906-7 · Cited by 306 · see citing works

Methanol-based industrial biotechnology: current status and future perspectives of methylotrophic bacteria

Schrader, J., Schilling, M., Holtmann, D., Sell, D., Filho, M. V., Marx, A., & Vorholt, J. A. (2008) · Trends in biotechnology · doi:10.1016/j.tibtech.2008.10.009 · Cited by 299 · see citing works

Converting Escherichia coli to a Synthetic Methylotroph Growing Solely on Methanol

Chen, F. Y.-H., Jung, H.-W., Tsuei, C.-Y., & Liao, J. C. (2020) · Cell · doi:10.1016/j.cell.2020.07.010 · Cited by 292 · see citing works

BIOLOGY OF AEROBIC CARBON MONOXIDE-OXIDIZING BACTERIA

Meyer, O. O., & Schlegel, H. G. (1983) · Annual Review of Microbiology · doi:10.1146/annurev.mi.37.100183.001425 · Cited by 284 · see citing works

Carbon Monoxide Specifically Inhibits Cytochrome C Oxidase of Human Mitochondrial Respiratory Chain

Alonso, J., Cardellach, F., López, S., Casademont, J., & Miró, Ò. (2003) · Pharmacology & Toxicology · doi:10.1034/j.1600-0773.2003.930306.x · Cited by 263 · see citing works

Dynamic response of RNA editing to temperature in Drosophila

Rieder, L. E., Savva, Y. A., Reyna, M. A., Chang, Y.-J., Dorsky, J. S., Rezaei, A., & Reenan, R. A. (2015) · BMC Biology · doi:10.1186/s12915-014-0111-3 · Cited by 243 · see citing works

C1-carbon sources for chemical and fuel production by microbial gas fermentation

Dürre, P., & Eikmanns, B. J. (2015) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2015.03.008 · Cited by 242 · see citing works

Carbon monoxide-dependent energy metabolism in anaerobic bacteria and archaea

Oelgeschläger, E., & Rother, M. (2008) · Archives of Microbiology · doi:10.1007/s00203-008-0382-6 · Cited by 236 · see citing works

Cofactor-dependent pathways of formaldehyde oxidation in methylotrophic bacteria

Vorholt, J. A. (2002) · Archives of Microbiology · doi:10.1007/s00203-002-0450-2 · Cited by 232 · see citing works

Barriers and opportunities in bio-based production of hydrocarbons

Zhou, Y. J., Kerkhoven, E. J., & Nielsen, J. (2018) · Nature Energy · doi:10.1038/s41560-018-0197-x · Cited by 213 · see citing works

Engineering Escherichia coli for methanol conversion

Müller, J. E. N., Meyer, F., Litsanov, B., Kiefer, P., Potthoff, E., Heux, S., Quax, W. J., Wendisch, V. F., Brautaset, T., Portais, J., et al. (2015) · Metabolic Engineering · doi:10.1016/j.ymben.2014.12.008 · Cited by 203 · see citing works

Pathways and Bioenergetics of Anaerobic Carbon Monoxide Fermentation

Diender, M., Stams, A. J. M., & Sousa, D. Z. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01275 · Cited by 203 · see citing works

Synthetic methylotrophy: engineering the production of biofuels and chemicals based on the biology of aerobic methanol utilization

Whitaker, W. B., Sandoval, N. R., Bennett, R. K., et al. (2015) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2015.01.007 · Cited by 201 · see citing works

The Mechanism of the Condensation of Formaldehyde with Tetrahydrofolic Acid

Kallen, R. G., & Jencks, W. P. (1966) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)96350-7 · Cited by 199 · see citing works

Molecular cloning and characterization of a gene coding for methanol oxidase inHansenula polymorpha

Ledeboer, A. M., Edens, L., Maat, J., et al. (1985) · Nucleic Acids Research · doi:10.1093/nar/13.9.3063 · Cited by 195 · see citing works

Formate Assimilation: The Metabolic Architecture of Natural and Synthetic Pathways

Bar‐Even, A. (2016) · Biochemistry · doi:10.1021/acs.biochem.6b00495 · Cited by 193 · see citing works

Using gas mixtures of CO, CO 2 and H 2 as microbial substrates: the do's and don'ts of successful technology transfer from laboratory to production scale

Takors, R., Kopf, M., Mampel, J., Bluemke, W., Blombach, B., Eikmanns, B. J., Bengelsdorf, F. R., Weuster‐Botz, D., & Dürre, P. (2018) · Microbial Biotechnology · doi:10.1111/1751-7915.13270 · Cited by 192 · see citing works

Engineering the biological conversion of methanol to specialty chemicals in Escherichia coli

Whitaker, W. B., Jones, J. A., Bennett, R. K., et al. (2016) · Metabolic Engineering · doi:10.1016/j.ymben.2016.10.015 · Cited by 186 · see citing works

In Vivo Assimilation of One-Carbon via a Synthetic Reductive Glycine Pathway in Escherichia coli

Yishai, O., Bouzon, M., Döring, V., & Bar‐Even, A. (2018) · ACS Synthetic Biology · doi:10.1021/acssynbio.8b00131 · Cited by 178 · see citing works

Improving carbon fixation pathways

Ducat, D. C., & Silver, P. A. (2012) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2012.05.002 · Cited by 170 · see citing works

Systems-level organization of yeast methylotrophic lifestyle

Rußmayer, H., Buchetics, M., Grünwald‐Gruber, C., Valli, M., Grillitsch, K., Modarres, G., Guerrasio, R., Klavins, K., Neubauer, S., Drexler, H., et al. (2015) · BMC Biology · doi:10.1186/s12915-015-0186-5 · Cited by 165 · see citing works

Assimilation, dissimilation, and detoxification of formaldehyde, a central metabolic intermediate of methylotrophic metabolism

Yurimoto, H., Kato, N., & Sakai, Y. (2005) · The Chemical Record · doi:10.1002/tcr.20056 · Cited by 164 · see citing works

Tuning a P450 Enzyme for Methane Oxidation

Zilly, F. E., Acevedo, J. P., Augustyniak, W., et al. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201006587 · Cited by 164 · see citing works

Yeast Methylotrophy: Metabolism, Gene Regulation and Peroxisome Homeostasis

Yurimoto, H., Oku, M., & Sakai, Y. (2011) · International Journal of Microbiology · doi:10.1155/2011/101298 · Cited by 163 · see citing works

Replacing the Calvin cycle with the reductive glycine pathway in Cupriavidus necator

Claassens, N. J., Bordanaba-Florit, G., Cotton, C. A. R., Maria, A. D., Finger‐Bou, M., Friedeheim, L., Giner-Laguarda, N., Palmer, M. M., Newell, W., Scarinci, G., et al. (2020) · Metabolic Engineering · doi:10.1016/j.ymben.2020.08.004 · Cited by 159 · see citing works

Methanol-essential growth of Escherichia coli

Meyer, F., Keller, P., Hartl, J., Gröninger, O. G., Kiefer, P., & Vorholt, J. A. (2018) · Nature Communications · doi:10.1038/s41467-018-03937-y · Cited by 158 · see citing works

Direct Conversion of Ethane to Ethanol by Engineered Cytochrome P450 BM3

Meinhold, P., Peters, M. W., Chen, M. M. Y., et al. (2005) · ChemBioChem · doi:10.1002/cbic.200500261 · Cited by 157 · see citing works

Genome-scale metabolic reconstructions and theoretical investigation of methane conversion in Methylomicrobium buryatense strain 5G(B1)

Torre, A. D. L., Metivier, A., Chu, F., Laurens, L. M. L., Beck, D. A. C., Pienkos, P. T., Lidstrom, M. E., & Kalyuzhnaya, M. (2015) · Microbial Cell Factories · doi:10.1186/s12934-015-0377-3 · Cited by 152 · see citing works

Engineering Corynebacterium glutamicum for methanol-dependent growth and glutamate production

Tuyishime, P., Wang, Y., Fan, L., Zhang, Q., Li, Q., Zheng, P., Sun, J., & Ma, Y. (2018) · Metabolic Engineering · doi:10.1016/j.ymben.2018.07.011 · Cited by 151 · see citing works

Escherichia coli is engineered to grow on CO2 and formic acid

Junho, B., Hwang, C. H., Ahn, J. H., et al. (2020) · Nature Microbiology · doi:10.1038/s41564-020-00793-9 · Cited by 148 · see citing works

Exploiting microbial hyperthermophilicity to produce an industrial chemical, using hydrogen and carbon dioxide

Keller, M. W., Schut, G. J., Lipscomb, G. L., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1222607110 · Cited by 140 · see citing works

Adaptive laboratory evolution of native methanol assimilation in Saccharomyces cerevisiae

Espinosa, M. I., González-García, R. A., Valgepea, K., Plan, M. R., Scott, C. S., Pretorius, I. S., Marcellin, E., Paulsen, I. T., & Williams, T. C. (2020) · Nature Communications · doi:10.1038/s41467-020-19390-9 · Cited by 131 · see citing works

Improving formaldehyde consumption drives methanol assimilation in engineered E. coli

Woolston, B. M., King, J. R., Reiter, M., Hove, B. V., & Stephanopoulos, G. N. (2018) · Nature Communications · doi:10.1038/s41467-018-04795-4 · Cited by 129 · see citing works

Scaffoldless engineered enzyme assembly for enhanced methanol utilization

Price, J. V., Chen, L., Whitaker, W. B., Papoutsakis, E. T., & Chen, W. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601797113 · Cited by 127 · see citing works

Assimilation of formic acid and CO 2 by engineered Escherichia coli equipped with reconstructed one-carbon assimilation pathways

Junho, B., & Lee, S. Y. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1810386115 · Cited by 127 · see citing works

Functional reconstitution of a bacterial CO2 concentrating mechanism in Escherichia coli

Flamholz, A. I., Dugan, E. J., Blikstad, C., Gleizer, S., Ben-Nissan, R., Amram, S., Antonovsky, N., Ravishankar, S., Noor, Ε., Bar‐Even, A., et al. (2020) · eLife · doi:10.7554/elife.59882 · Cited by 126 · see citing works

Biochemical and synthetic biology approaches to improve photosynthetic CO2-fixation

Erb, T. J., & Zarzycki, J. (2016) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2016.06.026 · Cited by 121 · see citing works

Core Catalysis of the Reductive Glycine Pathway Demonstrated in Yeast

de la Cruz, J. G., Machens, F., Messerschmidt, K., & Bar‐Even, A. (2019) · ACS Synthetic Biology · doi:10.1021/acssynbio.8b00464 · Cited by 120 · see citing works

Synthetic methanol auxotrophy of Escherichia coli for methanol-dependent growth and production

Chen, C.-T., Chen, F. Y.-H., Bogorad, I. W., Wu, T., Zhang, R., Lee, A. S., & Liao, J. C. (2018) · Metabolic Engineering · doi:10.1016/j.ymben.2018.08.010 · Cited by 118 · see citing works

Awakening a latent carbon fixation cycle in Escherichia coli

Satanowski, A., Dronsella, B. B., Noor, Ε., Vögeli, B., He, H., Wichmann, P., Erb, T. J., Lindner, S. N., & Bar‐Even, A. (2020) · Nature Communications · doi:10.1038/s41467-020-19564-5 · Cited by 118 · see citing works

Synthetic Methylotrophy: A Practical Solution for Methanol-Based Biomanufacturing

Wang, Y., Fan, L., Tuyishime, P., Zheng, P., & Sun, J. (2020) · Trends in biotechnology · doi:10.1016/j.tibtech.2019.12.013 · Cited by 117 · see citing works

Biological conversion of methane to methanol through genetic reassembly of native catalytic domains

Kim, H. J., Huh, J., Kwon, Y., et al. (2019) · Nature Catalysis · doi:10.1038/s41929-019-0255-1 · Cited by 116 · see citing works

Research Progress on the Indirect Hydrogenation of Carbon Dioxide to Methanol

Du, X., Jiang, Z. R., Su, D. S., & Wang, J. (2015) · ChemSusChem · doi:10.1002/cssc.201501013 · Cited by 115 · see citing works

Electrical-biological hybrid system for CO2 reduction

Tashiro, Y., Hirano, S.-I., Matson, M. M., Atsumi, S., & Kondo, A. (2018) · Metabolic Engineering · doi:10.1016/j.ymben.2018.03.015 · Cited by 112 · see citing works

Hansenula polymorpha

(2002) · Wiley eBooks · doi:10.1002/3527602356 · Cited by 106 · see citing works

Expression of the sub-pathways of the Chloroflexus aurantiacus 3-hydroxypropionate carbon fixation bicycle in E. coli: Toward horizontal transfer of autotrophic growth

Mattozzi, M. D., Ziesack, M., Voges, M. J. E. E. E., Silver, P. A., & Way, J. C. (2013) · Metabolic Engineering · doi:10.1016/j.ymben.2013.01.005 · Cited by 104 · see citing works

Expression of heterologous non-oxidative pentose phosphate pathway from Bacillus methanolicus and phosphoglucose isomerase deletion improves methanol assimilation and metabolite production by a synthetic Escherichia coli methylotroph

Bennett, R. K., Gonzalez, J. E., Whitaker, W. B., Antoniewicz, M. R., & Papoutsakis, E. T. (2017) · Metabolic Engineering · doi:10.1016/j.ymben.2017.11.016 · Cited by 101 · see citing works

Methanol as carbon substrate in the bio‐economy: Metabolic engineering of aerobic methylotrophic bacteria for production of value‐added chemicals

Pfeifenschneider, J., Brautaset, T., & Wendisch, V. F. (2017) · Biofuels Bioproducts and Biorefining · doi:10.1002/bbb.1773 · Cited by 100 · see citing works

Current advance in bioconversion of methanol to chemicals

Zhang, W., Song, M., Yang, Q., Dai, Z., Zhang, S., Xin, F., Dong, W., Ma, J., & Jiang, M. (2018) · Biotechnology for Biofuels · doi:10.1186/s13068-018-1265-y · Cited by 93 · see citing works

Biological carbon fixation: From natural to synthetic

Gong, F., Zhu, H., Zhang, Y., & Li, Y. (2018) · Journal of CO2 Utilization · doi:10.1016/j.jcou.2018.09.014 · Cited by 93 · see citing works

Highly active rubiscos discovered by systematic interrogation of natural sequence diversity

Davidi, D., Shamshoum, M., Guo, Z.-J., Bar-On, Y., Prywes, N., Oz, A., Jabłońska, J., Flamholz, A. I., Wernick, D. G., Antonovsky, N., et al. (2020) · EMBO Journal · doi:10.15252/embj.2019104081 · Cited by 93 · see citing works

Biocatalytic Conversion of Methane to Methanol as a Key Step for Development of Methane-Based Biorefineries

Hwang, I. Y., Lee, S. H., Choi, Y. S., et al. (2014) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1407.07070 · Cited by 87 · see citing works

Comparison of Fecal Collection Methods for Microbiota Studies in Bangladesh

Vogtmann, E., Chen, J., Kibriya, M. G., Chen, Y., Islam, T., Eunes, M., Ahmed, A., Naher, J., Rahman, A., Amir, A., et al. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.00361-17 · Cited by 81 · see citing works

Synthetic biology for CO2 fixation

Gong, F., Cai, Z., & Li, Y. (2016) · Science China Life Sciences · doi:10.1007/s11427-016-0304-2 · Cited by 79 · see citing works

Cloning and sequencing of the alcohol oxidase-encoding gene (AOD1) from the formaldehyde-producing asporogeneous methylotrophic yeast, Candida boidinii S2

Sakai, Y., & Tani, Y. (1992) · Gene · doi:10.1016/0378-1119(92)90708-w · Cited by 68 · see citing works

An engineered Calvin-Benson-Bassham cycle for carbon dioxide fixation in Methylobacterium extorquens AM1

von Borzyskowski, L. S., Carrillo, M., Leupold, S., Glatter, T., Kiefer, P., Weishaupt, R., Heinemann, M., & Erb, T. J. (2018) · Metabolic Engineering · doi:10.1016/j.ymben.2018.04.003 · Cited by 68 · see citing works

Bifunctional enzyme fusion of 3-hexulose-6-phosphate synthase and 6-phospho-3-hexuloisomerase

Orita, I., Sakamoto, N., Kato, N., et al. (2007) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-007-1023-8 · Cited by 65 · see citing works

Biological conversion of methanol by evolved Escherichia coli carrying a linear methanol assimilation pathway

Wang, X., Wang, Y., Liu, J., et al. (2017) · Bioresources and Bioprocessing · doi:10.1186/s40643-017-0172-6 · Cited by 61 · see citing works

Reduced mitochondrial malate dehydrogenase activity has a strong effect on photorespiratory metabolism as revealed by¹³C labelling

Lindén, P., Keech, O., Stenlund, H., Gardeström, P., & Moritz, T. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw030 · Cited by 57 · see citing works

Cloning and expression of the gene cluster encoding key proteins involved in acetyl-CoA synthesis in Clostridium thermoaceticum: CO dehydrogenase, the corrinoid/Fe-S protein, and methyltransferase

Roberts, D. L., James-Hagstrom, J. E., Garvin, D. K., Gorst, C. M., Runquist, J. A., Baur, J. R., Haase, F. C., & Ragsdale, S. W. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.1.32 · Cited by 56 · see citing works

Enhancement of malate production through engineering of the periplasmic rTCA pathway in Escherichia coli

Guo, L., Zhang, F., Zhang, C., et al. (2018) · Biotechnology and Bioengineering · doi:10.1002/bit.26580 · Cited by 49 · see citing works

The risks and benefits of low-dose cotrimoxazole prophylaxis for Pneumocystis pneumonia in renal transplantation.

Rm, H., Sl, B., Hopkin, J. M., et al. (1989) · PubMed · Cited by 48 · see citing works

A warm welcome for alternative CO 2 fixation pathways in microbial biotechnology

Claassens, N. J. (2016) · Microbial Biotechnology · doi:10.1111/1751-7915.12456 · Cited by 47 · see citing works

Binding of water to “Types I and II” Cu2+ in proteins

Boden, N., Holmes, M. C., & Knowles, P. F. (1974) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(74)90623-8 · Cited by 46 · see citing works

Integrated Metabolomics and Morphogenesis Reveal Volatile Signaling of the Nematode-Trapping Fungus Arthrobotrys oligospora

Wang, B.-L., Chen, Y.-H., He, J.-N., et al. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.02749-17 · Cited by 44 · see citing works

Applications of methylotrophs: can single carbon be harnessed for biotechnology?

Chistoserdova, L. (2018) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2018.01.012 · Cited by 43 · see citing works

Heterologous Expression of the Clostridium carboxidivorans CO Dehydrogenase Alone or Together with the Acetyl Coenzyme A Synthase Enables both Reduction of CO 2 and Oxidation of CO by Clostridium acetobutylicum

Carlson, E. D., & Papoutsakis, E. T. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.00829-17 · Cited by 41 · see citing works

Recent progress in metabolic engineering of microbial formate assimilation

Wen, M., Yuan, Q., Qi, H., Wang, Z., Ma, H., & Chen, T. (2020) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-020-10725-6 · Cited by 41 · see citing works

Functional Expression of the Clostridium ljungdahlii Acetyl-Coenzyme A Synthase in Clostridium acetobutylicum as Demonstrated by a NovelIn VivoCO Exchange Activity En Route to Heterologous Installation of a Functional Wood-Ljungdahl Pathway

Fast, A. G., & Papoutsakis, E. T. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.02307-17 · Cited by 39 · see citing works

Engineering of non-conventional yeasts for efficient synthesis of macromolecules: the methylotrophic genera

Houard, S. A., Heinderyckx, M., & Bollen, A. (2002) · Biochimie · doi:10.1016/s0300-9084(02)00011-1 · Cited by 35 · see citing works

Production of acrylic acid and propionic acid by constructing a portion of the 3-hydroxypropionate/4-hydroxybutyrate cycle from Metallosphaera sedula in Escherichia coli

Liu, Z., & Liu, T. (2016) · Journal of Industrial Microbiology & Biotechnology · doi:10.1007/s10295-016-1843-6 · Cited by 32 · see citing works

Nonlinear sequence-dependent structure of nigral dopamine neuron interspike interval firing patterns

Hoffman, R. E., Shi, W. X., & Bunney, B. S. (1995) · Biophysical Journal · doi:10.1016/s0006-3495(95)79882-4 · Cited by 30 · see citing works

Discovery and Biochemical Characterization of a Methanol Dehydrogenase From Lysinibacillus xylanilyticus

Lee, J., Park, S. H., Oh, S.-H., Lee, J.-J., Kwon, K. K., Kim, S. J., Choi, M., Rha, E., Lee, H., Lee, D., et al. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00067 · Cited by 27 · see citing works

Mixing and matching methylotrophic enzymes to design a novel methanol utilization pathway in E. coli

Simone, A. D., Vicente, C. M., Peiro, C., et al. (2020) · Metabolic Engineering · doi:10.1016/j.ymben.2020.07.005 · Cited by 25 · see citing works

Interactions among polymorphic and conserved residues in MHC class II proteins affect MHC-peptide conformation and T cell recognition

Tate, K. M., Lee, C., Edelman, S., et al. (1995) · International Immunology · doi:10.1093/intimm/7.5.747 · Cited by 22 · see citing works

Combined light and electron microscope in routine histopathology.

Jones, S. M., Chapman, S. K., Crocker, P. R., et al. (1982) · Journal of Clinical Pathology · doi:10.1136/jcp.35.4.425 · Cited by 15 · see citing works

Enhanced adenylate cyclase activity of turkey erythrocytes following treatment with β-adrenergic receptor antagonists

Peters, J. R., Nambi, P., Sibley, D. R., et al. (1984) · European Journal of Pharmacology · doi:10.1016/0014-2999(84)90089-x · Cited by 9 · see citing works

The gastrointestinal peptides and nutrition

Brown, J. C., McIntosh, C. H. S., & Pederson, R. A. (1983) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y83-043 · Cited by 4 · see citing works

[Comparative results of the treatment of gastroduodenal ulcers with low-energy laser and hyperbaric oxygenation].

Vv, K., Sinev, I. V., Gavrilenko, I. V., et al. (1985) · PubMed · Cited by 2 · see citing works

Henry P. Pendergrass, A.B., M.P.H., M.D.

Wyman, S. M. (1978) · Radiology · doi:10.1148/126.2.531 · Cited by 1 · see citing works

The story of malaria.

Covell, G. (1967) · PubMed · Cited by 1 · see citing works

[Orthodontic therapy using extraoral traction].

Dimitriadis, A. G. (1981) · PubMed · Cited by 1 · see citing works

[The effect of nibufin on reproductive function and the contraceptive effect of hormonal preparations].

Poskalenko, A. N., & Vv, B. (1973) · PubMed · Cited by 1 · see citing works

[Research on pasteurella infections in Bulgaria. IV. Sensitivity of strains of Pasteurella multocida to antibiotics and sulfonamides].

Tchentchev, I., & Mateev, M. (1966) · PubMed · Cited by 1 · see citing works

Presidential address: a personal testament--reflections on the Tower of Babel.

Wj, D. (1982) · PubMed · Cited by 1 · see citing works

[Cytodiagnosis from the surgical viewpoint. B. Use of cytodiagnosis in breast cysts].

Tohyama, T., & Takeshita, T. (1985) · PubMed · Cited by 1 · see citing works

[Cemento-dentinal relations. Microscopic and microradiographic aspects of the apical section and current therapeutical trends].

Nisenvaygue, S. (1979) · PubMed · Cited by 1 · see citing works

Living with rheumatoid arthritis.

Ae, F. (1980) · PubMed · Cited by 1 · see citing works

[Enzyme tests in the diagnosis of gynecologic diseases and in obstetrics].

Zaniewski, A. (1978) · PubMed · Cited by 1 · see citing works

[Management and nursing care of coma patients in a nursing home].

van Herwaarden, S. G., & Stoop, J. A. (1987) · PubMed · Cited by 1 · see citing works

Technologies and perspectives for achieving carbon neutrality

Wang, F., Harindintwali, J. D., Yuan, Z., Wang, M., Wang, F., Li, S., Yin, Z., Huang, L., Fu, Y., Li, L., et al. (2021) · The Innovation · doi:10.1016/j.xinn.2021.100180 · Cited by 1,330 · see citing works

Microbial Utilization of Next-Generation Feedstocks for the Biomanufacturing of Value-Added Chemicals and Food Ingredients

Zhang, C., Ottenheim, C., Weingarten, M., & Ji, L. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.874612 · Cited by 72 · see citing works

Recent Advances in Biocatalysis and Metabolic Engineering for Biomanufacturing

Lee, E. Y. (2019) · MDPI eBooks · doi:10.3390/books978-3-03921-575-1 · Cited by 1 · see citing works

The renaissance of yeasts as microbial factories in the modern age of biomanufacturing

Payen, C., & Thompson, D. A. (2019) · Yeast · doi:10.1002/yea.3439 · Cited by 9 · see citing works

Opportunities for yeast metabolic engineering: Lessons from synthetic biology

Krivoruchko, A., Siewers, V., & Nielsen, J. (2011) · Biotechnology Journal · doi:10.1002/biot.201000308 · Cited by 121 · see citing works

Impact of synthetic biology and metabolic engineering on industrial production of fine chemicals

Jullesson, D., David, F., Pfleger, B. F., & Nielsen, J. (2015) · Biotechnology Advances · doi:10.1016/j.biotechadv.2015.02.011 · Cited by 232 · see citing works