Skip to content
CiderHQ
Search

Organism

Brettanomyces anomalus

The second Brettanomyces species regularly recovered from cider and beer, less studied than B. bruxellensis but capable of the same phenolic chemistry.

Also called Dekkera anomala.

Kind
Yeast
Binomial
Brettanomyces anomalus
Role
Secondary fermentation, Spoilage

What it does

Conditions it works in

What the organism tolerates and what suppresses it. These are the levers a maker actually has: temperature, acidity, air, alcohol and sulphite.

Only the conditions a source states are listed. A missing row means no consulted source gave a figure, not that the condition is unimportant.
ConditionWhat is recorded
TemperatureRoughly 10–32 °C, with slow growth continuing at cellar temperature.
pHTolerates the whole cider range.
OxygenFacultative; favoured by low-level oxygen ingress.
Alcohol toleranceHigh, comparable with *B. bruxellensis* and above cider strength.
Sulphite toleranceSuppressed by molecular SO2 in the same pH-dependent way as *B. bruxellensis*; not reliably eliminated by it.

What it produces

Compounds this organism makes. Which organism made a compound usually decides whether it reads as a feature or as a symptom.

Faults it causes

Faults this organism is implicated in. Several are faults only against a particular expectation — the same activity is a signature elsewhere.

Where in the process it appears

About Brettanomyces anomalus

Brettanomyces anomalus — also written Dekkera anomala, the same teleomorph-anamorph pairing described in the bruxellensis record — is the less-studied of the two Brettanomyces species that turn up in fermented drinks. It has been isolated from beer, wine and cider, and it shares the phenolic metabolism that makes the genus notorious, but the quantitative work behind statements about ethylphenol yield has overwhelmingly been done on B. bruxellensis.

That imbalance in the literature is a reason for caution rather than for silence. It is fair to say that B. anomalus can produce ethylphenols, that it grows slowly in maturing and packaged cider, and that it is controlled by the same measures. It is not fair to transfer bruxellensis numbers to it, and this record does not.

In practice a cider maker will rarely distinguish the two without sequencing, and rarely needs to: the corrective actions are identical. Wood hygiene, minimised oxygen ingress, attention to molecular SO2 rather than to total sulphite, and — where a cider is intended to be free of the character — removal of the organism before packaging.

What people ask next

Questions readers ask about the things this page mentions. Each one goes to the section that answers it rather than to a page written to receive the question.

Where to go next

Sources

What this page rests on. Where a source is marked as registered rather than read, CiderHQ is recording that the body is authoritative on the subject without claiming to have worked through the document itself. See our evidence policy for what each state means.