SPRI 2006 - SUGAR PROCESSING CONFERENCE
The Dr. Margaret A. Clarke Award
for
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September 19, 2006
Award Winner for the
Best Paper at the SPRI Conference.
DR GILLIAN EGGLESTON
USDA/ARS/SRRC
NEW ORLEANS, LA, USA
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The Dr. Margaret A. Clarke Award for Best Paper presented at the
International SPRI Conference on Sugar Processing Research, was presented by
Mr. Robert O. Hatch, Chairman of SPRI to Dr. Gillian Eggleston, Lead Scientist,
representing USDA-ARS-SRRC, New Orleans, Louisiana, USA, at the Grande Hotel
São Pedro, in Águas de São Pedro, Brazil, on
September 19, 2006.
SPRI wishes to thank Dr. Gillian Eggleston and co-authors, Dr. Henrique Amorim and S.C. de Lima Paulillo
with Fermentec Ltda, Brazil,
Dr. Luis C. Basso, and Tiago O. Basso, with the Universidade
de São Paulo, Brazil, for their remarkable work presented at this year SPRI
Conference on Sugar Processing Research with the theme “Frontiers in
Sugar Processing Research,” in Águas de São
Pedro, Brazil. As the sugar industry
moves forward with new processing and diversifying sugar research in sugarcane,
sugarbeet and ethanol production we were pleased to congratulate Dr. Gillian
Eggleston and co-authors in their interest and dedication as frontiers in a new
age of sugar processing. Abstract of
paper presented is listed below.
ABSTRACT OF THE BEST PAPER PRESENTED
Mannitol as a Sensitive
Indicator of Sugarcane Deterioration and Bacterial Contamination in Fuel
Alcohol Production, Gillian Eggleston1, L. C.
Basso2, H. Amorim3, S. C De Lima Paulillo3 and
T. O. Basso2 1 USDA-ARS-SRRC, c/o Agronomy Dept., Louisiana State Univ.,
Baton Rouge, LA, USA. 2Universidade de São Paulo
, Piracicaba , São Paulo
, Brazil , 3Fermentec,
Piracicaba , São Paulo , Brazil
Mannitol, formed mainly by Leuconostoc
mesenteroides bacteria, is a very sensitive
indicator of sugarcane deterioration that can predict processing problems. A
rapid (4 to 7 min) enzymatic method has been developed to measure mannitol in juice pressed from consignments of sugarcane
delivered to the factory. This screening tool will allow factory staff to
rapidly know which consignments of cane will affect processing negatively or
reject consignments that will cause unacceptable processing problems. This
method can be easily performed using existing equipment in sugarcane factories,
with mannitol being measured spectrophotometrically
using mannitol dehydrogenase
as the enzyme catalyst. The stability of the reagents, limited cane juice
preparation, linearity, accuracy and precision are described. The method is
highly specific for mannitol and was not affected by
the presence of sucrose, glucose, fructose, or dextran.
The current cost is only ~60 U.S. cents per analysis. Mannitol
has also been proven to be an advantageous indicator of bacterial contamination
- one of the main factors causing drops in fuel alcohol fermentation yields as
well as yeast (Saccharomyces) flocculation and
foaming problems. Compared to other indicators, mannitol
is not produced by yeast cells, only contaminating bacteria (mostly some
Lactobacillus strains) during fermentation; its concentration is directly
associated with bacterial activity, and it can be measured easily. A strong
correlation existed between mannitol formation and
bacteria counts in sugarcane juice and molasses fermentations with induced
bacterial contaminations.
