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Metabolism of aroma bacteria as related to diacetyl production

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Title Metabolism of aroma bacteria as related to diacetyl production
Names Brown, Ruth Elaine (creator)
Sandine, William E. (advisor)
Date Issued 1967-09-01 (iso8601)
Note Graduation date: 1968
Abstract Factors influencing diacetyl production by the aroma bacteria
Leuconostoc citrovorum and Streptococcus diacetilactis were investigated.
When grown in association with lactic streptococci, L. citrovorum
strain 91404 decreased in cell numbers from 10⁸ to 10⁶ over
two weeks of daily subculturing in sterile non-fat milk incubated at
21°C. The ability to produce diacetyl over this period also was lost
by L. citrovorum, but the reduction in cell numbers did not appear
responsible because it was also shown that 2.5 X 10⁴ cells were able
to produce detectable diacetyl after one transfer. Disk assay procedures
did not reveal any antibiotic activity by the lactic streptococci
against Leuconostoc. The enrichment of milk with 100 μg/ml sodium citrate, 100 μg/ml sodium pyruvate, 10% yeast extract or
50% pea extract did not enhance diacetyl production by L. citrovorum.
The addition of 0.125 ppm MnSO₄ caused enhanced diacetyl production
up to 12 hours and enhanced diacetyl reduction from 12 to 24 hours by L. citrovorum grown in association with lactic streptococci.
The cell-free extracts prepared from these Mn⁺⁺ supplemented
cultures of L. citrovorum had 14 times more diacetyl reductase
activity than non-treated cultures. Diacetyl production by
S. diacetilactis 18-16 was not enhanced by MnSO₄ and flavor reduction
was increased only slightly; diacetyl reductase activity was not
affected. Treatment of the milk with 0.03% H₂O₂ and sufficient
0.004% catalase to decompose the H₂O₂ resulted in at least twice
as much diacetyl production by S. diacetilactis 18-16; the resulting
flavor also was stable. This treatment did not increase cell numbers,
decrease diacetyl reductase activity or enhance respiration
as measured by manometry studies. Diacetyl plus acetoin was synthesized
by the cell-free extracts of L. citrovorum 91404 and S. diacetilactis 18-16 when supplemented with 0.1 μmole acetyl CoA
plus 0.1 μmole pyruvate in the presence of catalytic amounts of Mn⁺⁺ and TPP. S. diacetilactis also produced diacetyl plus acetoin
from a acetolactic acid plus 0.1 μmole acetyl CoA. The synthetic
activity of the extracts was not reduced by MnSO₄ addition or stimulated
by H₂O₂-catalase treatment. From the results it was clear
that important differences exist between the aroma bacteria with
regard to optimum requirements for diacetyl production.
Genre Thesis/Dissertation
Topic Streptococcus
Identifier http://hdl.handle.net/1957/46986

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