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Table 3 Typical examples for metabolic engineering of plants and microorganisms for enhanced production of anthocyanins

From: Biotechnological advances for improving natural pigment production: a state-of-the-art review

Target compound

Hosts

Strategies

Substrate

Yield

Year

References

Pelargonidin 3-O-glucoside (P3G)

Cyanidin 3-O-glucoside (C3G)

E. coli

Introduction of F3H, DFR, ANS and 3GT

Naringenin, eriodictyol

5.6 μg/L, 6.0 μg/L

2005

Yajun et al. (2005)

PEG and C3G

E. coli

Gene screening, enhancement of UDP-glucose supply, culture medium pH adjustment, protein fusion

Afzelechin, catechin

78.9 mg/L of P3G, 70.7 mg/L of C3G

2007

Yan et al. (2008)

C3G

E. coli

Improvement of catechin uptake and C3G secretion; increase of ANS and 3GT expression; enhanced intracellular availability of UDP-glucose; optimization of culture and induction conditions

Catechin

350 mg/L

2015

Lim et al. (2015)

P3G

E. coli

Polycultures; 15 exogenous enzymes from diverse sources were divided into four E. coli strains

Glucose

9.5 mg/L

2017

Jones et al. (2017)

C3G

E. coli

Promoter engineering for balancing ANS and 3GT expression

Catechin

439 mg/L

2019

Shrestha et al. (2019)

Pyranoanthocyanins

E. coli

Co-culture of 4-vinylphenol or 4-vinylcatechol producing E. coli strains with cyanidin-3-O-glucoside producer recombinant E. coli

Catechin

19.5 mg/L of pyranocyanidin-3-O-glucoside-phenol, and 13 mg/L of pyranocyanidin-3-O-glucoside-catechol

2019

Akdemir et al. (2019)

Total anthocyanin

Tomato

Expression of the Delila (Del) and Rosea1 (Ros1) genes from the snapdragon Antirrhinum majus

/

2.83 mg/g (fresh weight)

2008

Butelli et al. (2008)

C3G

Corynebacterium

glutamicum

Expression optimization of ANS and 3GT, improved UDP-glucose availability, process optimization

Catechin

40 mg/L

2018

Zha et al. (2018)

P3G, C3G, and delphinidin-3-O-glucoside (D3G)

S. cerevisiae

Gene screening, construction of the whole biosynthetic pathway of anthocyanins from glucose

Glucose

1–2 mg/L

2018

Eichenberger et al. (2018)

P3G

S. cerevisiae

Gene screening, genomic integration, deletion of EXG1 and SPR1, abolishing formation of phloretic acid, cultivation optimization

Glucose

0.001 µmol/g DCW

2018

Levisson et al. (2018)