跳至主要内容

Genetically Engineered E. coli Cranks Out Opiate Precursor

 Though opiate drug use has been much maligned over the past several years, the need for medically relevant painkillers has not waned. Scientists have been continually on the hunt for improved production methods of opiate compounds, as extraction from poppy sap is inefficient and time-consuming.

    Now, a team of Japanese researchers from Ishikawa Prefectural University and Kyoto University has modified several genes from Escherichia coli to produce large quantities of the morphine precursor thebaine, which can be changed to make painkilling drug compounds. Moreover, the investigators found that their engineered E. coli produced 300 times more thebaine compared to a recently developed method involving yeast, in addition to having a much lower risk of unregulated production.

    “Morphine has a complex molecular structure; because of this, the production of morphine and similar painkillers is expensive and time-consuming,” explained co-author Fumihiko Sato, Ph.D., professor in the graduate school of biostudies at Kyoto University. “But with our E. coli, we were able to yield 2.1 milligrams of thebaine in a matter of days from roughly 20 grams of sugar, as opposed to 0.0064 mg with yeast.”

    The findings from this study were published recently in Nature Communications through an article entitled “Total biosynthesis of opiates by stepwise fermentation using engineered Escherichia coli.”

    Traditionally, morphine is extracted from poppy sap in a process that results in opiates such as thebaine and codeine. In order to streamline the production process, synthetic biologists had recently engineered the yeast genome so that it produced opiate alkaloids from sugar. However, there were ethical concerns that the pain-killing molecules could be produced easily and unregulated, provided that one has access to the necessary yeast strain. The authors of the current study suggest that such a risk is almost insignificant with the newly engineered E. coli strains.

    “Four strains of genetically modified E. coli are necessary to turn sugar into thebaine,” noted Dr. Sato. “E. coli are more difficult to manage and require expertise in handling. This should serve as a deterrent to unregulated production.”

    Previously, the Japanese team tweaked E. coli to synthesize reticuline, another morphine precursor that appears upstream in the transformation process from thebaine. In the new system, the team added genes from other bacteria and enzyme genes from opium poppies, Coptis japonica, and Arabidopsis. The researchers credit the strong activity of enzymes in the new system for their success in making thebaine and hope to achieve even further improvements.

    “By adding another two genes, our E. coli were able to produce hydrocodone, which would certainly boost the practicality of this technique,” Dr. Sato stated. “With a few more improvements to the technique and clearance of pharmaceutical regulations, manufacturing morphine-like painkillers from microbes could soon be a reality.”

评论

此博客中的热门博文

What is preclinical testing?

In the process of  preclinical testing  of a compound or biological agent into a drug, the compound involved must go through the testing phase. First, we need to identify potential targets that can treat the disease. Then, a variety of compounds or preparations are screened out. Any compound that has shown potential as a drug for the treatment of this disease needs to be tested for toxicity before clinical testing to reduce the possibility of injury. preclinical testing What is the basis of preclinical testing? According to US Food and Drug Administration (FDA) regulations, a series of tests are required before a new drug is approved for use. In the first stage, basic research determines a hypothetical target for the treatment of a certain disease, and then screens small molecules or biological compounds to discover any substance with the potential to treat the disease. Then, a  preclinical research  phase followed, before which, as described above, the potential toxicity of the compou

Inventory of the three major in vitro pharmacokinetic research methods

  The metabolic properties of a compound are an essential factor in whether or not it can be used as a drug in the clinical setting, so pharmacokinetic studies of newly synthesized compounds are required in drug development. In vitro incubation with liver microsomes, recombinant CYP450 enzyme lines, and in vitro incubation with hepatocytes are some of the more common in vitro drug metabolism methods. 1. In vitro incubation method with liver microsomes The metabolic stability and metabolic phenotypes of candidate compounds in different species of liver microsomes are good predictors of the metabolic properties of compounds in vivo. They are practical tools for evaluating candidate compounds in the pre-development phase of drug development. Liver microsomes include rat liver microsomes, human liver microsomes, canine liver microsomes, monkey liver microsomes, and mouse liver microsomes. In in vitro incubation of the liver, microsomes are the "gold standard" for in vitro d

Enzyme Activity Assay Service

  Enzymatic assay Lance Assay Alphascreen Assay Z’-LYTE Assay Adapta Assay Kinase-Glo Assay ADP-Glo Assay Ligand Binding Assay ELISA Assay HTRF Assay Enzyme activity assays  are laboratory methods for measuring enzymatic activity. They are vital for the study of enzyme kinetics and enzyme inhibition. Enzyme units : Amounts of enzymes can either be expressed as molar amounts, as with any other chemical, or measured in terms of activity, in enzyme units. Medicilon provides various  enzyme activity assays  for  kinases , phosphatases, proteinases, deacetylase, peptidase, esterase, and other enzymes. Our line of well-characterized immunoassays and biochemical kits ensures accurate and reproducible results. Enzyme is a  large category of bio-molecules  that catalyze various biological processes including metabolic processes, cellular signaling and regulation, cell division and apoptosis. Enzymatic reactions convert substrate molecules into chemically modified molecules products with high sp