Enhancing Lithium-Ion Battery Longevity Through Chemical Modifications

Lithium-ion battery technology

Lithium-ion Batteries: A Path to Extended Lifespan

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Recent studies suggest that the lifespan of lithium-ion batteries can be extended using standard, cost-effective chemicals.

Lithium-ion batteries feature a porous separator sandwiched between a negative electrode and a positive electrode, immersed in an electrolyte that facilitates the movement of lithium ions during charging and discharging.

At the negative electrode, the electrolyte decomposes to create a thin protective coating that enhances battery stability and longevity.

Wang Chunsheng explains that forming a similar protective layer on the cathode has traditionally been challenging due to differing electrical conditions, which create a reactive environment that causes conventional electrolytes to break down before a stable coating can form, according to researchers from the University of Maryland.

Wang and his team utilized a straightforward reaction from organic chemistry to tackle this issue. This reaction enhances the electrolyte’s electron acceptance, inducing a controlled decomposition process that forms a stable protective coating on the cathode.

“By meticulously controlling the molecular decomposition of the electrolyte, we can precisely dictate the protective layer that forms on the cathode,” states Zhang Xiyue, a postdoctoral researcher in Wang’s group.

This flexibility in chemical reactions allows the resulting cathode-electrolyte layer to be tailored for enhanced protection, which could either provide strong shielding or design for faster electrochemical reactions, optimizing batteries for maximum power or extended life.

“If we can guarantee the formation of the cathode-electrolyte layer, it represents a significant advancement toward achieving longer battery cycles,” asserts Michel Armand from the CIC energiGUNE research center in Spain. Given that Wang and his colleagues modified the battery design using established chemical techniques, this new battery should be both safe and easy to manufacture, according to Armand.

While it remains uncertain exactly how much this innovative approach can extend the lifespan of lithium-ion batteries, further clarity is anticipated as the technology develops.

“This is a relatively simple modification to existing battery technology,” Wang notes. “After thorough safety and long-cycle testing, this approach could indeed reach consumers.”

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Source: www.newscientist.com

The E. coli Genome Redesigned with 101,000 DNA Modifications

E. coli can lead to serious illnesses, yet is frequently utilized in pharmaceutical development.

Victor Habbick Visions/Science Photo Library

Unlike the natural evolution of life forms, our ability to create life has reached new heights. The genome of an E. coli bacterium has been meticulously redesigned via computer simulations, utilizing just 57 out of the 64 genetic codons. This synthetic genome was built from the ground up and introduced into living bacterial cells.

“This was a massive undertaking,” states Wesley Robertson from the Institute of Medical Research in Molecular Biology, Cambridge, UK.

The objective was to demonstrate the feasibility of this approach, with the 57 codons, termed Syn57, offering commercial applications. Future modifications could enable Syn57 to develop complete resistance to viral infections, a significant benefit for the industrial production of proteins used in pharmaceuticals, food, or cosmetics. Since viral proteins depend on their hosts to produce, altering the genetic code can lead to erroneous viral proteins.

Moreover, additional modifications permit Syn57 to synthesize proteins containing up to 27 amino acids, whereas natural proteins are limited to 20. These synthetic proteins hold potential for functions unattainable with conventional proteins.

A protein is essentially a sequence of amino acids arranged in a specified order determined by a gene. Each triplet of DNA bases, known as a codon, instructs the synthesis machinery on when to add the next amino acid or when to cease the protein assembly.

There are four DNA bases that combine to produce 64 distinct codons. However, organisms on Earth typically utilize only 20 amino acids, leading to considerable redundancy, with multiple codons corresponding to each amino acid.

If all instances of a specific codon for an amino acid were substituted with another codon for the same amino acid, that original codon could then be repurposed. For instance, it could code for non-natural amino acids or alternative chemicals, facilitating the creation of novel protein types.

Theoretically, only 21 unique codons are required, allowing for a biological organism to free up to 43 codons—one for each natural amino acid and one stop codon. However, this is not yet feasible, as increasing genetic alterations raises the likelihood of harmful unintended consequences.

Instead, biologists are taking a more measured approach. In 2011, an edit of 314 genes in E. coli aimed to free one codon.

Because executing thousands of genetic edits is so labor-intensive, Robertson and his team opted to synthesize the DNA from scratch. In 2019, they introduced Syn61, incorporating 18,000 changes across 4 million DNA bases, achieving the release of three codons in the E. coli genome. A derivative company named Constructive.Bio is working on commercial applications.

Currently, researchers are implementing 101,000 modifications to release seven codons within Syn57. This process necessitated testing small sections of the reconstructed genome on live bacterial cultures to identify and rectify harmful changes. This complex procedure was repeated with progressively larger genome fragments until the entire structure was reassembled.

“This marks a significant achievement, resulting from years of effort,” mentions Akos Nyerges at Harvard Medical School. Nyerges’ team is also working to release seven codons in E. coli via different codon reproductions. “Our journey with the 57 codons in E. coli is ongoing,” he adds.

While Syn57 is already fully established, its growth rate is significantly slower than that of typical strains. Enhancements in this aspect are essential for commercial viability. “We anticipate being able to improve the growth rates, making it more beneficial,” remarks Robertson.

For the time being, his focus will be on investigating the potential applications of Syn57 rather than attempting further codon releases. “There’s still a great deal to accomplish before contemplating even more compressed genetic codes,” he concludes.

The first synthetic genome bacteria were created in 2010, but their design aimed more at simplifying organisms than at codon recovery.

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Source: www.newscientist.com

Polycystic Ovary Syndrome May Be Inherited Through Chemical Modifications of DNA

Illustration of enlarged ovaries in an individual with polycystic ovary syndrome

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Polycystic ovarian syndrome (PCOS) may be transmitted through families via chemical markers that modify DNA structure, implying that medications that adjust these markers in embryos could potentially prevent the disorder.

Individuals with PCOS usually display at least two of the following three key traits: elevated levels of male hormones like testosterone, irregular menstrual cycles, and the presence of immature eggs that resemble cysts in the ovaries.

While this condition frequently runs in families, its inheritance pattern remains unclear. “Around 25-30 genetic mutations are associated with PCOS, but they only account for a minor part of the hereditary aspects,” explains Elisabet Stener-Victorin from the Karolinska Institute in Sweden.

Research on mice indicates that variations in epigenetic marks (chemical tags that regulate gene activity without changing DNA sequences) may also be influential. As eggs develop, most of these marks are believed to be erased, but some may persist as a possible means of inheritance.

To investigate this in relation to human PCOS, Qianshu Zhu from China’s Chungin Medical University and colleagues conducted an analysis of the epigenetic markers in eggs and embryos donated 3 days prior, revealing data from 133 and 95 PCOS donors respectively. “No one has truly explored this with human samples,” states Stener-Victorin.

The study revealed a correlation between PCOS donation and altered patterns in three epigenetic marks in eggs and embryos. Two of these marks contribute to silencing genes and helping to package them within cells, resulting in a tighter DNA coil around a protein called histone, rendering the genetic code less accessible for RNA transcription, a crucial step in protein synthesis. Meanwhile, the third type of mark activates genes by loosening the DNA coil.

Together, the epigenetic modifications related to PCOS could potentially affect the metabolic processes of eggs and embryos, thereby elevating the chances of passing on PCOS to the next generation. Nevertheless, more research is essential to understand how these changes influence PCOS symptoms in offspring, both in mice and humans, as noted by Stener-Victorin. “At this stage, I recognize these marks differ, and that doesn’t inherently mean they are harmful,” she remarks.

Additional experiments suggest that the researchers may employ medications to reverse epigenetic alterations, potentially mitigating the risk of PCOS. “If we observe that modifying these histone marks changes the next-generation characteristics of PCOS, it could present a critical prevention target,” Zhu stated in a press release. Furthermore, the team posits that clinicians might utilize PCOS-related epigenetic markers to choose the healthiest embryos during in vitro fertilization procedures.

Zhu presented these findings at the European Breeding Association’s Annual Meeting held in Paris on July 1st.

topics:

  • Epigenetics/
  • Women’s health

Source: www.newscientist.com