2015
DOI: 10.1016/j.lwt.2015.06.065
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Screening of microorganisms for bioconversion of (+)-valencene to (+)-nootkatone

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Cited by 27 publications
(17 citation statements)
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“…The total oxidation rate of (+)-valencene to terpenoids by PK2-32 reached as 49.1% (mol mol À1 ), which was higher than that by Y. lipolytica 2-2ab previously reported. 8 However, strain PK2-33 containing ADH3 showed decreases for both b-nootkatol and (+)-nootkatone production compared to PK2-32. ADH1 is generally regarded as primarily responsible for the NAD + regeneration from NADH through the acetaldehyde reduction, [32][33][34] which is benecial for the b-nootkatol oxidation to (+)-nootkatone.…”
Section: (+)-Valencene Hydroxylation Using Resting Cellsmentioning
confidence: 89%
See 1 more Smart Citation
“…The total oxidation rate of (+)-valencene to terpenoids by PK2-32 reached as 49.1% (mol mol À1 ), which was higher than that by Y. lipolytica 2-2ab previously reported. 8 However, strain PK2-33 containing ADH3 showed decreases for both b-nootkatol and (+)-nootkatone production compared to PK2-32. ADH1 is generally regarded as primarily responsible for the NAD + regeneration from NADH through the acetaldehyde reduction, [32][33][34] which is benecial for the b-nootkatol oxidation to (+)-nootkatone.…”
Section: (+)-Valencene Hydroxylation Using Resting Cellsmentioning
confidence: 89%
“…Previously, (+)-valencene extracted from Valencia orange was converted into (+)-nootkatone by biotransformation using Aspergillus, Rhodococcus, Chlorella, Mucor species Botryodiplodia theobromae 1368, Yarrowia lipolytica 2.2ab, and Phanerochaete chrysosporium. 1,8 These reported biotransformation approaches suffered frequently from long reaction time, relatively low yields and troublesome purication procedures. 9 Recent rapid developments in metabolic engineering by rewiring cellular metabolism provide an attractive alternative approach for producing plant terpenoids.…”
Section: Introductionmentioning
confidence: 99%
“…Currently, most flavor compounds are obtained by chemical synthesis [ 2 ], which have the disadvantages of a high energy consumption and pollution [ 3 ]. The products obtained through chemical synthesis cannot be considered as “natural” products [ 4 ]. With the increasing awareness of the link between diet and health, consumers prefer products labelled as “natural” or “bio-flavors” [ 5 ].…”
Section: Introductionmentioning
confidence: 99%
“…The research on the transformation of nootkatone by Y. lipolytica was shown in the Table 1. Palmerín‐Carreno et al studied about microorganisms for bioconversion of (+)‐valencene to (+)‐nootkatone in different phase system (Table 1) (Palmerin‐Carreno, et al., 2016; Palmerín‐Carreño et al., 2015; Palmerin‐Carreno et al., 2016). Guo et al constructed synthetic pathway of (+)‐ nootkatone in Y. lipolytica by heterologous expression of CnVS and CYP706M1 (Table 1) (Guo et al., 2018).…”
Section: Introductionmentioning
confidence: 99%