Green Carbon co-organizes 17th International Clostridium Conference

http://qibebt.cas.cn/news/zyxw/202409/t20240922_7378447.html

From September 19th to 22nd, the 17th International Clostridium Conference was held in Qingdao, hosted by the International Clostridium Conference Organizing Committee, supported by the Bioenergy Research Laboratory of Qingdao Institute of Energy, the Key Laboratory of Solar Photovoltaic Conversion and Utilization, Shandong Energy Research Institute, and Qingdao New Energy Shandong Provincial Laboratory, and co-organized by the One Carbon Biotechnology Research Center and Green Carbon Editorial Department.

Since 1990, the International Clostridium Conference has been held every two years, and this Clostridium Conference is the second time to be held in China. On the afternoon of the 19th, the executive chairman of the conference, Researcher Li Fuli, director of the One Carbon Biotechnology Research Center, announced the opening of the conference. Director Lv Xuefeng delivered a speech on behalf of the Qingdao Institute of Energy and introduced the construction and development of the institute to the delegates.

This conference invited about 150 scholars and guests from domestic and foreign academic and business circles to attend the conference, including more than 50 foreign experts from Germany, the United States, France, South Korea, the United Kingdom, Italy and other countries. The conference was divided into four parts according to the topic direction: physiology and systems biology, genetics and synthetic biology, metabolic engineering and raw material utilization, industry and new applications. More than 40 oral speakers shared the latest research results with the participants, discussed future research directions, and exchanged problems and challenges encountered in Clostridium research and industrialization engineering.

As a valuable platform for scientific exchange and cooperation, this conference will further promote the development of Clostridium research. At the same time, the successful holding of this conference is of great significance to enhancing the influence of the institute in the field of Clostridium research. (Text/Photo by Ma Xiaoqing)

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https://doi.org/10.1016/j.biortech.2025.133788

http://english.cas.cn/newsroom/research_news/life/202601/t20260114_1145714.shtml

Breweries typically monitor fermentation by analyzing broth composition. Alcohols, esters, acids and residual sugars are quantified via chromatography-based assays. While reliable, these tests are time-consuming and only yield batch-average results.

A research led by scientists from the CAS Qingdao Institute of Bioenergy and Bioprocess Technology (QIBEBT) has simplified this process and developed a novel workflow dubbed “process ramanomics,” which is based on spontaneous single-cell Raman spectroscopy.

To validate the approach, the researchers tracked an industrial beer fermentation process using the lager yeast Saccharomyces pastorianus, sampling a single production batch over an eight-day period. At each stage of fermentation, they collected high-throughput Raman spectra from individual cells (a “ramanome”) and matched these unique molecular fingerprints to conventional lab measurements of 43 extracellular phenotypes in the fermentation medium.

Using multivariate regression analysis, the team found that ramanomes could accurately predict 19 extracellular phenotypes. This included four higher alcohols, four esters, four amino acids, two organic acids, four mono- and disaccharide substrates, and the alcohol-to-ester ratio—a commonly used indicator tied to beer flavor balance. In practical terms, a single, rapid cellular analysis can now replace multiple time-intensive chemical assays—without sacrificing single-cell resolution details.

Because the models output cell-level predictions, the researchers also tracked phenotypic heterogeneity over time. Different metabolite classes displayed distinct heterogeneity trajectories, and for several phenotypes higher heterogeneity tended to accompany lower metabolite levels—suggesting that dispersion among cells may be a useful process-state indicator.

http://english.qibebt.cas.cn/ne/rp/202512/t20251201_1134324.html

UNESCO’s “Decade of Sciences” aims to engage science in achieving its sustainable development goals (SDGs).

UNESCO  has just endorsed the long-standing commitment of the Qingdao Institute of Bioenergy and Bioprocess Technology QIBEBT to providing open science solutions for green and sustainable technologies.

QIBEBT’s “Green Carbon Programme” focuses on four core themes,

  • development and utilization of green carbon resources,
  • green conversion and utilization of fossil carbon resources,
  • efficient fixation and utilization of carbon emissions, and
  • analysis and management of multi-scale carbon cycles.

In addition, QIBEBT operates the editorial office of the Green Carbon journal https://www.sciencedirect.com/journal/green-carbon which offers an in-depth and multidisciplinary view of research advances in the field.

With the leverage of the UNESCO endorsement, QIBEBT will boost its efforts to drive innovation and improve public science literacy, supporting high-quality, sustainable, and low-carbon development in China and worldwide for achieving the SDGs.

https://www.sciencedirect.com/science/article/pii/S2950155525000667?via%3Dihub

https://www.cas.cn/syky/202511/t20251125_5089765.shtml

A research team at the CAS Tianjin Institute of Industrial Biotechnology has proposed a novel artificial carbon fixation pathway—LATCH which comprises 10 completely known enzymatic steps. Each cycle converts two molecules of HCO₃⁻ into one molecule of acetyl-CoA, requiring only adenosine triphosphate (ATP) and reduced coenzyme II for energy. Kinetic and thermodynamic modeling analysis shows that it is a linear autocatalytic cycle structure without kinetic traps or thermodynamic barriers, possessing high feasibility and potential for continued development. It can provide insights for improving the efficiency of systems such as photosynthetic microorganisms, plants, and engineered cell factories.

Regarding the selection of parental modules, the research team referenced research on the serine cycle and designed a modified version of the serine cycle, simplifying the pathway structure and bypassing the inefficient steps involving hydroxypyruvate, thus enabling the pathway to function effectively in the heterologous host *E. coli*. Simultaneously, the team replaced the amino acid deamination and transamination steps in the serine cycle with a decarboxylation process, forming an MCG cycle free from formic acid dependence. This cycle can further convert glycerate 3-phosphate produced by processes such as the Calvin cycle and glycolysis into acetyl-CoA in a negative carbon mode. The study also referenced a series of photorespiration bypass concepts developed for recovering the Rubisco byproduct glycolate-2-phosphate, among which the TaCo module, due to its artificial carboxylation reaction, theoretically has a maximum yield of 150%. This study found that by introducing glyoxylate reductase as a key step to act as a “molecular latch,” the natural serine cycle and the artificially carboxylated module TaCo can be recombined, resulting in a functional transformation—from two parent modules dependent on organic substrates to a complete carbon-fixing cycle.

Based on the LATCH cycle formed by module integration, kinetic analysis shows that this pathway is a linear autocatalytic cycle, theoretically avoiding kinetic traps while eliminating the need to establish complex regulatory relationships. Meanwhile, eight steps in the pathway receive thermodynamic support from adenosine triphosphate (ATP), reducing power, or high-energy substrates, and the remaining two lyase-catalyzed processes do not pose thermodynamic bottlenecks. These inherent advantages at the stoichiometric, kinetic, and thermodynamic levels lay the foundation for the continued development and application of LATCH.

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