Nav: Home

Genes behind lager yeast's cold- and sugar-loving success revealed

January 30, 2019

MADISON, Wis. -- Lager beer is cold, crisp, dry -- and worth about half a trillion dollars worldwide.

Behind the world's most popular alcoholic beverage is a yeast adapted to the cold, and hungry for the sugars it will transform into bubbles and booze.

That yeast is a hybrid, an amalgamation of the domesticated baker's yeast Saccharomyces cerevisiae and a recently discovered wild species, Saccharomyces eubayanus. Hundreds of years ago, the two species combined their strengths into a cold-fermenting strain that readily produces the crisp, light taste that came to dominate the beer market in the centuries that followed.

In a pair of new papers, University of Wisconsin-Madison Professor of Genetics Chris Todd Hittinger, his graduate student EmilyClare Baker and others show how modern lager yeast adopted the cold-loving and sugar-hungry traits essential to their success.

In one paper, to be published Feb. 1 in Science Advances, the team demonstrates that when the cold-loving S. eubayanus donated its mitochondria -- the power-generating portion of the cell -- to the new hybrid, it conferred cold tolerance on the strain. Today, all industrial lager strains retain the S. eubayanus mitochondria and ferment at cold temps.

In a second paper, Baker and Hittinger investigated the ability of S. eubayanus to ferment all the sugars in wort, the barley malt extract that ferments into beer. Most strains of S. eubayanus cannot ferment maltotriose, the second-most common sugar in wort. But the researchers were able to evolve a brand-new protein capable of transporting maltotriose into the cell, revealing a potential path to more aggressive fermentation of all available sugars, a key trait in producing a dry, crisp beer. The paper was published on the pre-print server bioRxiv ahead of publication in the journal PLOS Genetics.

The new research is the first to identify the genetic underpinnings of how two of the most defining features of lager production -- cold tolerance and complete fermentation -- evolved in S. eubayanus and its hybrid offspring. Hittinger and Baker have applied for patents based on their work, which could provide new opportunities for altering both the temperature range and sugar metabolizing ability of industrial lager strains.

In 2011, Hittinger was part of the team that first isolated S. eubayanus in the wild from forests in Patagonia. Since then, his lab has worked to uncover how S. eubayanus combined with the bread-and-ale yeast S. cerevisiae some 500 years ago to kickstart the behemoth lager beer industry. Their partners in the brewing industry and the UW-Madison food science department helped them zero in on researching the origin of two key traits: growth in the cold and churning through all the sugar in wort.

One clue to lager yeast's cold preference came from a slate of recent studies showing that temperature tolerance in a wide range of species could be linked, at least partially, to mitochondria. These cellular components generate the bulk of the energy that cells rely on and have their own genome, albeit a small one with just a handful of genes.

Baker and Hittinger had previously shown that lager yeast inherited their mitochondria from S. eubayanus. To see if these mitochondria helped lager yeast thrive at cold temperatures, Baker treated S. eubayanus or S. cerevisiae strains with a chemical that broke down the yeast's mitochondrial DNA.

"Some yeasts are able to dispense with their mitochondrial genome," says Baker, now a postdoctoral researcher at the University of Oregon. "As a result, you can get this blank slate strain without a mitochondrial genome and use that for crosses."

By making crosses between the two yeast species with or without their mitochondria intact, Baker produced two sets of hybrids: one had mitochondria from S. cerevisiae, the other from S. eubayanus. Other than the origin of their mitochondria, the hybrids were identical.

When Baker tested the growth of these hybrids at different temperatures, the differences were immediately apparent. The yeast with S. eubayanus mitochondria tolerated cold but wilted in the heat; strains with S. cerevisiae mitochondria couldn't handle the cold.

"At the most extreme temperatures, it's basically the difference between growing and not growing," says Hittinger, who is also a member of the Department of Energy-supported Great Lakes Bioenergy Research Center headquartered at UW-Madison.

"For the first time we can remake custom lager strains that have the S. cerevisiae mitochondrial genome. And when you do that you get shifted temperature preferences," says Hittinger. "This is a new category of brewing strains that right now is not in anyone's arsenal. And we think it very well could have novel properties in beer production."

Cold-loving lager yeast take a long time to ferment and require refrigeration, which makes lager production more expensive than brewing ales. Hittinger and Baker believe that shifting lager production to slightly warmer temperatures with tailored mitochondria could produce huge cost savings -- as long as the distinctive lager taste is preserved.

But some brewers are looking to move beyond the traditional lager. Since S. eubayanus was discovered in 2011, brewers have tried to brew beer with the wild yeast in hopes of creating a new market. Heineken has released a limited-edition S. eubayanus beer and the Wisconsin Brewing Company in Verona, Wisconsin, is trying to do the same in partnership with the Hittinger lab.

However, S. eubayanus cannot ferment all of the sugar in wort. Most strains of the yeast lack the ability to transport the sugar maltotriose into the cell to digest. Because maltotriose is the second-most common sugar in wort, brewing with S. eubayanus can result in an overly sweet beer.

So Baker and Hittinger tried to evolve better use of maltotriose in S. eubayanus strains. Over several months, the researchers grew S. eubayanus with plenty of maltotriose and a dash of other, digestible sugars -- just enough to let the yeast slowly reproduce. Then they looked for any yeast that gained the ability to transport and ferment maltotriose.

More than 2,000 generations later, they found a single strain that could grow on the sugar. When they looked at the yeast's genome, they found a new gene. The yeast had combined chunks of two genes capable of transporting maltose -- a sugar related to maltotriose but smaller and easier to transport.

"And that was particularly interesting because neither of these genes was able to transport maltotriose by themselves, but this new chimeric gene was," says Baker.

By reconfiguring existing genes, the yeast strain was able to quickly evolve a new trait without having to accumulate many slow, random mutations.

"We're hopeful that this will provide a way to reduce the sugar content in the final product," says Hittinger. "It'll make pure S. eubayanus beers less cloying and drier, more like a conventional lager, but will still retain some of the wild character that you expect from this wild, cold-tolerant strain."

Hittinger's office boasts empty bottles of Heineken's S. eubayanus beers and he's looking forward to seeing more of the wild beers available. His group is now working with brewers to test the new yeast strains under realistic conditions.

"This is a really interesting basic science story about how you take the different capabilities of two species that diverged from one another millions of years ago, hybridize them together, and get the best of both worlds to eventually create a multibillion-dollar industry," says Hittinger.
-end-
--Eric Hamilton, (608) 263-1986, eshamilton@wisc.edu

This work was supported by the USDA National Institute of Food and Agriculture (Hatch project no. 1003258), the National Science Foundation (grant no. DEB-1253634), the Department of Energy Great Lakes Bioenergy Research Center (DOE BER Office of Science; nos. DE-SC0018409 and DE-FC02-07ER64494) and the National Institutes of Health (grant no. GM080669).

CONTACT: Chris Todd Hittinger, cthittinger@wisc.edu; EmilyClare Baker, emilyclare@me.com

University of Wisconsin-Madison

Related Mitochondria Articles:

Mitochondria-targeted antioxidant SkQ1 helps to treat diabetic wounds
Members of the Faculty of Biology and A.N. Belozersky Institute of Physico-Chemical Biology, a unit of the Lomonosov Moscow State University, have tested on a mouse model a mitochondria-targeted antioxidant, helping to treat diabetic wounds.
Mitochondria targeting anti-tumor compound
Researchers from Kumamoto University in Japan have found that the compound folic acid-conjugated methyl-BETA-cyclodextrin (FA-M-BETA-CyD) has significant antitumor effects on folate receptor-ALPHA-expressing (FR-ALPHA (+)) cancer cells.
Closing the gate to mitochondria
A team of researchers develops a new method that enables the identification of proteins imported into mitochondria.
Elucidated connection between renal failure and 'bad' mitochondria described
Biologists from the A.N. Belozersky Institute of Physico-Chemical Biology, a unit of the Lomonosov Moscow State University suggested the approach to prevent kidney injury after ischemia.
How exercise -- interval training in particular -- helps your mitochondria stave off old age
Researchers have long suspected that the benefits of exercise extend down to the cellular level, but know relatively little about which exercises help cells rebuild key organelles that deteriorate with aging.
Cell disposal faults could contribute to Parkinson's, study finds
A fault with the natural waste disposal system that helps to keep our brain cell 'batteries' healthy may contribute to neurodegenerative disease, a new study has found.
Sex cells evolved to pass on quality mitochondria
Mammals immortalize their genes through eggs and sperm to ensure future generations inherit good quality mitochondria to power the body's cells, according to new UCL research.
Newly identified pathway in mitochondria fuels tumor progression across cancer types
Scientists at The Wistar Institute have identified a novel protein pathway across several types of cancer that controls how tumor cells acquire the energy necessary for movement, invasion and metastasis.
Collapse of mitochondria-associated membrane in ALS
Mitochondria-associated membrane (MAM) is a contacting site of endoplasmic reticulum and mitochondria, and plays a key role in cellular homeostasis.
New research on the muscles of elite athletes: When quality is better than quantity
A Danish-Swedish research team working on a project led by University of Southern Denmark has discovered that muscle endurance is not only determined by the number of mitochondria, but also their structure.

Related Mitochondria Reading:

Best Science Podcasts 2019

We have hand picked the best science podcasts for 2019. Sit back and enjoy new science podcasts updated daily from your favorite science news services and scientists.
Now Playing: TED Radio Hour

Anthropomorphic
Do animals grieve? Do they have language or consciousness? For a long time, scientists resisted the urge to look for human qualities in animals. This hour, TED speakers explore how that is changing. Guests include biological anthropologist Barbara King, dolphin researcher Denise Herzing, primatologist Frans de Waal, and ecologist Carl Safina.
Now Playing: Science for the People

#SB2 2019 Science Birthday Minisode: Mary Golda Ross
Our second annual Science Birthday is here, and this year we celebrate the wonderful Mary Golda Ross, born 9 August 1908. She died in 2008 at age 99, but left a lasting mark on the science of rocketry and space exploration as an early woman in engineering, and one of the first Native Americans in engineering. Join Rachelle and Bethany for this very special birthday minisode celebrating Mary and her achievements. Thanks to our Patreons who make this show possible! Read more about Mary G. Ross: Interview with Mary Ross on Lash Publications International, by Laurel Sheppard Meet Mary Golda...