Armillaria luteovirens Sacc |
2011 |
optimization of various conditions |
production of 5
|
[108] |
Inonotus obliquus
|
2012 |
optimization of various conditions |
69.37 mg/L of 8
|
[109] |
Inonotus obliquus
|
2014 |
yield increase with aqueous extract and methanol extract from birch bark |
increased production of 8
|
[110] |
Saccharomyces cerevisiae
|
2014 |
insertion and expression regulation of genes |
5 from 0.01 to 1.92 mg L−1 OD−1
|
[112] |
Saccharomyces cerevisiae
|
2015 |
changes in intracellular supply of NADPH/oxygen |
1.5 and 3.2 times higher production of 5
|
[113] |
Gal80p mutant of Saccharomyces cerevisiae
|
2016 |
up-regulation of the expressed genes |
0.16 mg/L/OD600 of 5
|
[104] |
Saccharomyces cerevisiae
|
2016 |
increase in the supply of squalene |
8.23 mg/L of 9
|
[114] |
Saccharomyces cerevisiae CEN.PK BA4 |
2017 |
usage of excess of ethanol |
182 mg/L of 5
|
[115] |
|
2017 |
|
|
[116] |
Phaeodactylum tricornutum
|
2019 |
introduction of Lotus japonicus oxidosqualene cyclase and Medicago truncatula cytochrome P450 with native reductase |
production of 8 and 9
|
[117] |
Escherichia coli and Saccharomyces cerevisiae
|
2019 |
usage of optimized lupeol pathway genes |
production of 9
|
[118] |
Yarrowia lipolytica
|
2019 |
usage of glycerol as a starting material |
26.53 mg/L of 5
|
[120] |
Yarrowia lipolytica
|
2019 |
systematic metabolic engineering |
204.89±11.56 mg/L of triterpenoids (23.71% of 5) |
[121] |
Saccharomyces cerevisiae
|
2019 |
usage of RoCYP01 (CYP716A155) |
yields of 5 higher than 1 g/L |
[106] |
various yeast strains |
2020 |
SCRaMbLE technique |
production of 5
|
[122] |