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. 2022 Jun 15;2022:9871087. doi: 10.34133/2022/9871087

Table 1.

Transporter applications in microbial cell factories.

Transporter Species Compound Function Reference
Substrates
Gal2p S. cerevisiae Xylose Improved the transport rate and accelerated utilization of xylose. [40]
AraT S. cerevisiae L-arabinose Transported L-arabinose with high specificity and high affinity. [36]
XylE P. putida Xylose Broadened metabolic capacity towards new substrates. [43]
GatA S. cerevisiae D-galacturonic acid Achieved coutilization of D-galUA and D-glucose. [44]
Lac12 S. cerevisiae Lactose Increased uptake of the lactose. [6668]
Intermediate metabolites
ShiA E. coli 3-Dehydroshikimate Enhanced reuptake of intermediate metabolite from extracellular to cytoplasm. [45]
FadL E. coli Palmitate Achieved reuptake of excreted intermediate metabolite. [69]
Δpxa1 S. cerevisiae Fatty acyl-CoA Increased production of fatty acyl-CoA in the cytoplasm. [46]
NtJAT1, NtMATE2 S. cerevisiae Tropine Alleviated vacuolar intermediate metabolite transport limitations. [47]
Target products
AcrE, MdtE, MdtC E. coli Medium-chain fatty acid Increased extracellular MCFA concentration by 59.7%, 43.2%, and 83.1%. [55]
FATP1 S. cerevisiae Fatty alcohol Enabled an increased cell fitness for fatty alcohol production. [56]
FATP1 S. cerevisiae 1-Alkenes Improved the extracellular and total 1-alkene production. [57]
MacA, TolC, MacB E. coli 6-Deoxyerythronolide B Increased the 6dEB titers. [60]
Orf14, Orf3 Burkholderia Epothilones Raised the ratio of extracellular to intracellular accumulation from 9.3 : 1 to 13.7 : 1. [62]
TolC, AcrB E. coli amorphadiene Increased yield by 46%. [59]
AcrA, TolC AcrB, E. coli Kaurene Increased yield by 82%. [59]
Snq2p S. cerevisiae β-Carotene Improved β-carotene secretion level by 4.04-fold. [64]
AcrAB E. coli Limonene Reduced limonene toxicity. [70]
Bfr1 S. cerevisiae Caffeine Enhanced cellular resistance to caffeine. [34]
AbPUP1, AbLP1 S. cerevisiae Littorine and hyoscyamine Exported vacuolar littorine and hyoscyamine to the yeast cytosol. [37]
AtDTX1 E. coli Reticuline Achieved the secretion of high levels of reticuline. [65]
MttA A. niger cis-aconitic acid Secreted 9.8 g/L aconitic acid after 240 h of cultivation. [71]
Spmae S. cerevisiae L-malic acid Increased the accumulation. [50]
AtABCG29 S. cerevisiae Coumaryl alcohol Increased cellular tolerance to p-coumaryl alcohol. [72]
PtPTP Phaeodactylum tricornutum Pyruvate Enhanced biomass, lipid contents, and growth. [73]
DCT1 A. niger Malic acid Improved malic acid production by 36.8%. [74]
MTT Y. lipolytica Itaconic acid Enhanced itaconic acid titer by 10.5-folds. [75]
RibM B. subtilis Riboflavin and roseoflavin Increased the production of riboflavin and roseoflavin. [76]
PP_1271 P. putida Propionic acid Improved cellular tolerance to PA. [48]
YbjE Synechococcus sp Lysine Generated a large pool of lysine in the extracellular media. [77]
Qdr3 S. cerevisiae Muconic acid Increased cellular tolerance to glutaric, adipic, muconic, and glutaconic acid. [78]
CexA A. niger Citric acid Enhanced the secretion of citric acid. [79]
M2 E. coli Proton Increased acid tolerance. [80]
SerE C. glutamicum L-serine Increased L-serine efflux. [51]
Tpo2p S. cerevisiae cis,cis-muconic acid, protocatechuic acid Improved the production of target compound. [39]