Integrated Automation for Continuous High-Throughput Synthetic Chromosome Assembly and Transformation to Identify Improved Yeast Strains for Industrial Production of Biofuels and Bio-based Chemicals

Author(s):  
Stephen R. Hughes ◽  
Steven B. Riedmuller
2020 ◽  
Vol 52 (12) ◽  
pp. 1420-1426
Author(s):  
Mingyue Fei ◽  
Xudan Mao ◽  
Yiyang Chen ◽  
Yalan Lu ◽  
Lin Wang ◽  
...  

Abstract β-Alanine (3-aminopropionic acid) holds great potential in industrial application. It can be obtained through a chemical synthesis route, which is hazardous to the environment. It is well known that l-aspartate-α-decarboxylase (ADC) can convert l-aspartate to β-alanine in bacteria. However, due to the low activity of ADC, industrial production of β-alanine through the green biological route remains unclear. Thus, improving the activity of ADC is critical to reduce the cost of β-alanine production. In this study, we established a dual-fluorescence high-throughput system for efficient ADC screening. By measuring the amount of β-alanine and the expression level of ADC using two different fluorescence markers, we can rapidly quantify the relative activity of ADC variants. From a mutagenesis library containing 2000 ADC variants, we obtained a mutant with 33% increased activity. Further analysis revealed that mutations of K43R and P103Q in ADC significantly improved the yield of β-alanine produced by the whole-cell biocatalysis. Compared with the previous single-fluorescence method, our system can not only quantify the amount of β-alanine but also measure the expression level of ADC with different fluorescence, making it able to effectively screen out ADC variants with improved relative activity. The dual-fluorescence high-throughput system for rapid screening of ADC provides a good strategy for industrial production of β-alanine via the biological conversion route in the future.


2019 ◽  
Vol 29 (1) ◽  
pp. 133-149
Author(s):  
Khosro Balilashaki ◽  
Hedayat Zakizadeh ◽  
Jamal Ali Olfati ◽  
Maryam Vahedi ◽  
Anuj Kumar ◽  
...  

With recent advances in high-throughput sequencing (HTS) technologies to improve plants, there is a need to release orchid specific genomic resources and platforms that are crucial for managing omics elements in systematic manner. Authors provide details about the recent developments in biotechnological techniques, genomics, transcriptomics, proteomics, metabolomics and their applications for the industrial production, propagation, conservation and manipulation of Phalaenopsis orchid. Plant Tissue Cult. & Biotech. 29(1): 133-149, 2019 (June)


2014 ◽  
Vol 6 (7) ◽  
pp. 685-693 ◽  
Author(s):  
Xianjie Kang ◽  
Lingli Jiang ◽  
Xi Chen ◽  
Haiyu Yuan ◽  
Chunxiong Luo ◽  
...  

With a simple but robust well-based microfluidic device, we can high-throughput load and trace dozens of different budding yeast strains at single cell level simultaneously, providing precise cell information such as cell size, cell cycle, protein localization and protein expression level.


2013 ◽  
Vol 62 (1) ◽  
pp. 67-72 ◽  
Author(s):  
BARBARA STACHOWIAK

Astaxanthin is a xanthophill pigment with commercial application in the aquaculture, pharmaceutical, food and cosmetic industries. The red yeast Xanthophyllomyces dendrorhous is one of the most promising microorganisms for its industrial production. However, astaxanthin content in wild yeast strains is low. Pigment production by X. dendrorhous can be improved by mutagenesis. The aim of the study was to assess the efficiency of four mutagens: UV radiation, benomyl, ethyl methanesulfonate and ethidium bromide in generating asthaxanthin-hyperproducing strains of the yeast Xanthophyllomyces dendrorhous DSM 5626. Mutations with benomyl, ethidium bromide and UV radiation generated a group of hyperpigmented mutants exhibiting increases up to 100% in astaxanthin content. Ethyl methanesulfonate turned out to be useless in this respect.


2020 ◽  
Vol 11 ◽  
Author(s):  
Molly K. Burke ◽  
Kaitlin M. McHugh ◽  
Ian C. Kutch

Random spore analysis (RSA) is a classic method in yeast genetics that allows high-throughput purification of recombinant haploid spores following specific crosses. RSA typically involves a number of steps to induce sporulation, purge vegetative cells that fail to sporulate, and disrupt the ascus walls of sporulated cells to release haploid spores. These steps generally require expensive chemicals and/or enzymes that kill diploid cells but have few effects on spores. In the fission yeast Schizosaccharomcyes pombe, heat shock has been reported as an effective addition to RSA protocols, but to our knowledge heat shock has not been used for this purpose in the budding yeast Saccharomyces cerevisiae. Here, we evaluate the effects of heat shock on vegetative and sporulated cultures of four diverse yeast strains: a European wine strain (DBVPG6765), a Japanese sake strain (Y12), a West African palm wine strain (DBVPG6044) and a North American strain isolated from the soil beneath an oak tree (YPS128). We characterize this phenotype under multiple combinations of temperature and incubation time, and find specific conditions that lead to the exclusion of vegetative cells and an enrichment in spores, which differ by strain. We also collected genome sequence data from a recombinant population that experienced multiple rounds of RSA, including one round with a heat shock treatment. These data suggest that when incorporated into an RSA protocol, heat shock leads to increased genetic diversity among the cells that survive and mate. Ultimately, our work provides evidence that short heat treatments can improve existing RSA protocols, though in a strain-specific manner. This result informs applications of high-throughput RSA protocols, such as QTL mapping and experimental evolution research.


2020 ◽  
Vol 11 ◽  
pp. 100532
Author(s):  
Marlous van Dijk ◽  
Ignis Trollmann ◽  
Margarete Alice Fontes Saraiva ◽  
Rogelio Lopes Brandão ◽  
Lisbeth Olsson ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Cristian Varela ◽  
Caroline Bartel ◽  
Damian Espinase Nandorfy ◽  
Anthony Borneman ◽  
Simon Schmidt ◽  
...  

2020 ◽  
Vol 8 (7) ◽  
pp. 1034 ◽  
Author(s):  
Dana Byrtusová ◽  
Volha Shapaval ◽  
Jiří Holub ◽  
Samuel Šimanský ◽  
Marek Rapta ◽  
...  

Beta (β)–glucans are polysaccharides composed of D-glucose monomers. Nowadays, β-glucans are gaining attention due to their attractive immunomodulatory biological activities, which can be utilized in pharmaceutical or food supplementation industries. Some carotenogenic Basidiomycetes yeasts, previously explored for lipid and carotenoid coproduction, could potentially coproduce a significant amount of β–glucans. In the present study, we screened eleven Basidiomycetes for the coproduction of lipids and β–glucans. We examined the effect of four different C/N ratios and eight different osmolarity conditions on the coproduction of lipids and β–glucans. A high-throughput screening approach employing microcultivation in microtiter plates, Fourier Transform Infrared (FTIR) spectroscopy and reference analysis was utilized in the study. Yeast strains C. infirmominiatum CCY 17-18-4 and R. kratochvilovae CCY 20-2-26 were identified as the best coproducers of lipids and β-glucans. In addition, C. infirmominiatum CCY 17-18-4, R. kratochvilovae CCY 20-2-26 and P. rhodozyma CCY 77-1-1 were identified as the best alternative producers of β-glucans. Increased C/N ratio led to increased biomass, lipid and β-glucans production for several yeast strains. Increased osmolarity had a negative effect on biomass and lipid production while the β-glucan production was positively affected.


Author(s):  
Andreas Burn ◽  
Christian Heger ◽  
Stephan Buecheler ◽  
Lukas Greuter ◽  
Patrick Reinhard ◽  
...  

Author(s):  
Natthida Sophon ◽  
Choladda Phiwpesh ◽  
Sieng Darith ◽  
Wichai Cherdshewasart ◽  
Chuenchit Boonchird

Abstract A yeast estrogen screening (YES) assay was improved to increase sensitivity for detection of phytoestrogens. New yeast strains minus one or the other of transporters Pdr5 or Snq2 and harboring yEGFP as a reporter gene were developed. The new strains showed 2–100 fold improvement in sensitivity for detection of standard estrogens and anti-estrogens. In addition, the assay time (1h) using the newly developed strains was shorter than that (4h) previously reported. Furthermore, the snq2-minus strains were most effective for detection of estrogenic activity while the pdr5-minus strains were most effective for detection of anti-estrogenic activity. The efficacy of the new methods was evaluated and confirmed by testing with 23 Thai medicinal plant species. The new strains were also tested for detection of xenoestrogens. The results revealed that the newly developed YES methods were specific and rapid and suitable for simple high-throughput screening or detection of estrogen-like compounds.


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