Biotechnological methods for chalcone reduction using whole cells of Lactobacillus, Rhodococcus and Rhodotorula strains as a way to produce new derivatives
Microbial strains of the genera Dietzia , Micrococcus , Pseudomonas , Rhodococcus , Gordonia , Streptomyces , Pseudomonas , Bacillus , Penicillium , Rhodotorula and Lactobacillus were screened for the ability to convert chalcones. Synthesis of chalcones was performed by the Claisen-Schmidt reaction....
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Published in: | Applied microbiology and biotechnology Vol. 100; no. 19; pp. 8371 - 8384 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Berlin/Heidelberg
Springer Berlin Heidelberg
01-10-2016
Springer Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | Microbial strains of the genera
Dietzia
,
Micrococcus
,
Pseudomonas
,
Rhodococcus
,
Gordonia
,
Streptomyces
,
Pseudomonas
,
Bacillus
,
Penicillium
,
Rhodotorula
and
Lactobacillus
were screened for the ability to convert chalcones. Synthesis of chalcones was performed by the Claisen-Schmidt reaction. There were three groups of chalcones obtained as the products, which included the derivatives containing 4-substituted chalcone, 2′-hydroxychalcone and 4′-methoxychalcone. The B ring of the chalcones was substituted in the
para
position with different groups, such as halide, hydroxyl, nitro, methyl, ethyl and ethoxy one. The structure–activity relationship of the tested chalcones in biotransformation processes was studied. It has been proven that Gram-positive bacterial strains
Rhodococcus
and
Lactobacillus
catalyzed reduction of C=C bond in the chalcones to give respective dihydrochalcones. The strain
Rhodotorula rubra
AM 82 transformed chalcones into dihydrochalcones and respective secondary alcohols. These results suggest that the probiotic strain of
Lactobacillus
can be used for biotransformations of chalcones, which has not been described before. The structure of new metabolites
14a
and
15b
were established as 4-ethoxy-4′-methoxydihydrochalcone and 3-(4-bromophenyl)-1-(4′-
O
-methylphenyl)-2-propan-1-ol, respectively, which was confirmed by
1
H NMR and
13
C NMR analysis. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0175-7598 1432-0614 |
DOI: | 10.1007/s00253-016-7607-4 |