Yeast brew up anti-malarials

Bioengineers program the microbe to produce artemisinin precursor -- and at potentially lower cost, they argue

| 3 min read

Register for free to listen to this article
Listen with Speechify
0:00
3:00
Share
Bioengineers have programmed yeast to produce a precursor to the potent antimalarial drug artemisinin, they report in this week's Nature. They argue that the engineered cells, if scaled up to industrial-sized batches, could pump out the drug efficiently and for less than it costs to extract it from plants, currently the only source of the drug.Malaria is now resistant to the older and far cheaper drug chloroquine, making artemisinins "the most effective antimalarial drugs we have," Nick White, director of research in Southeast Asia for Wellcome Trust, told The Scientist. "Development of an inexpensive yeast source which could be scaled up for industrial production is very exciting."Artemisinins are currently produced using the Chinese herb wormwood (Artemisia annua), cultivated in Africa and its native China. However, the plant must grow for two years before harvest and then yields only 1% of its dry weight in artemisinins, according to White, who did not participate in the current study.During the study, the researchers, led by Jay Keasling at the University of California in Berkeley, boosted the activities of several genes and dampened the activity of another to bias a biosynthetic pathway in a strain of yeast. By manipulating regulatory elements that control the genes, they tweaked the pathway to maximize the output of one of its products, farnesyl pyrophosphate. Then they added a wormwood enzyme that converts the pyrophosphate to amorphadiene, which can be oxidized to their goal: artemisinic acid, a precursor to artemisinin.That's when they hit their first stroke of good luck. "We were assuming a worst case scenario: That we would need to clone out three enzymes" for the final three-step oxidation, Keasling told The Scientist. It turned out that a single plant enzyme did the trick. They found a cytochrome P450 enzyme that converts nearly all of the amorphadiene to artemisinic acid, with little remaining of the alcohol and aldehyde intermediates.Their final stroke of luck came when they discovered that the yeast secrete the artemisinic acid, which sticks to the outside of the cells and can be washed off with an alkaline rinse. "It essentially self-purified," Keasling said. Production costs should be even lower without the need to open the cells and sort the acid out from all the proteins and other metabolites, he added.Despite their good fortune, getting all the elements to work as a coordinated circuit was no easy feat, said synthetic biologist Chris Voigt of the University of California in San Francisco, who did not participate in the work. "They have developed new ways of controlling the expression of enzymes which required the beautiful combination of regulatory elements to really control every step of this pathway," Voigt told The Scientist. "It's a whole slew of advances." Although Keasling's group has previously reported preliminary progress toward their goal, "this is really the first time you can imagine the production of this molecule having a huge impact," Voigt said.Malaria kills more than a million people each year, mostly in the developing world. Previous efforts to wipe out the disease have failed. Still, artemisinins alone are no panacea, White warned -- for instance, the drugs must be used in combination with another to minimize the chance a second wave of drug resistance. But getting the drugs for cheaper is still crucial to controlling the disease, White said. "Current treatment depends on them."Susan Brown sbrown@the-scientist.comLinks within this articleD-K Ro, et al, "Production of the antimalarial drug precursor artemisinic acid in engineered yeast." Nature, April 12, 2006. http://www.nature.comP. Silver and J. Way, "Cells by design," The Scientist, September 27, 2004. http://www.the-scientist.com/article/display/14950/Wellcome Trust South-East Asia Programme http://www.wellcome.ac.uk/doc_WTD003485.htmlJ. Parry, "Taking a new look at an ancient tradition," The Scientist, May 9, 2005. http://www.the-scientist.com/article/display/15463Jay Keasling http://www.cchem.berkeley.edu/jdkgrp/J. Lucentini, "Is this life?" The Scientist, January, 2006. http://www.the-scientist.com/article/display/18854/Chris Voigt http://www.voigtlab.ucsf.eduB. Daviss, "Malaria, science, and social responsibility," The Scientist, March 28, 2005. http://www.the-scientist.com/article/display/15349World Health Organization Global Malaria Programme http://www.who.int/malaria/
Interested in reading more?

Become a Member of

The Scientist Logo
Receive full access to more than 35 years of archives, as well as TS Digest, digital editions of The Scientist, feature stories, and much more!
Already a member? Login Here

Meet the Author

  • Susan Brown

    This person does not yet have a bio.
Share
TS Digest January 2025
January 2025, Issue 1

Why Do Some People Get Drunk Faster Than Others?

Genetics and tolerance shake up how alcohol affects each person, creating a unique cocktail of experiences.

View this Issue
Sex Differences in Neurological Research

Sex Differences in Neurological Research

bit.bio logo
New Frontiers in Vaccine Development

New Frontiers in Vaccine Development

Sino
New Approaches for Decoding Cancer at the Single-Cell Level

New Approaches for Decoding Cancer at the Single-Cell Level

Biotium logo
Learn How 3D Cell Cultures Advance Tissue Regeneration

Organoids as a Tool for Tissue Regeneration Research 

Acro 

Products

Bio-Rad Logo

Bio-Rad Extends Range of Vericheck ddPCR Empty-Full Capsid Kits to Optimize AAV Vector Characterization

An illustration of different-shaped bacteria.

Leveraging PCR for Rapid Sterility Testing

Conceptual 3D image of DNA on a blue background.

Understanding the Nuts and Bolts of qPCR Assay Controls 

Bio-Rad
Takara Bio

Takara Bio USA Holdings, Inc. announces the acquisition of Curio Bioscience, adding spatial biology to its broad portfolio of single-cell omics solutions