Table 3.
Bacteria | Yeasts/Fungi | Remarkable metabolic traits defining sensorial properties of aguamiel or pulque | References |
---|---|---|---|
Lactobacillus sp. Leuconostoc mesenteroides, L. dextranicum Zymomonas mobilis | Saccharomyces cerevisiae | Essential microorganisms responsible for acid (lactic acid), alcoholic and production of EPS | Sánchez-Marroquín and Hope, 1953; Sánchez-Marroquín et al., 1957 |
Yeasts isolated from aguamiel: Candida lusitaneae, Klyuveromyces marxianus var bulagricus (+), S. cerevisiae Yeast isolated from pulque: C. valida (+), S. cerevisiae (chevalieri), S. cerevisiae (capensis), K. marxianus var lactis (+) | Several isolates of C. valida, S. cerevisiase (chevalier) isolated from pulque were able to resist to >10% of alcohol. Potential relevance in ethanol production during the fermentation and resistance to killer toxins | Estrada-Godina et al., 2001 | |
Acetobacter aceti, A. aceti subsp. xylinus, Bacillus simplex, B. subtilis, Cellulomonas sp., Escherichia sp., Kokuria rosea, Lactobacillus sp., L. delbrueckii, L. vermiforme, Leuconostoc sp., L. mesenteroides subsp. dextranicum, L. mesenteroides subsp. mesenteroides, Macrococcus caseolyticus, Micrococcus luteus, Sarcina sp., Z. mobilis subsp. mobilis | Cryptococcus sp., Candida parapsilosis, Clavispora lusitaniae, Debaryomyces carsonii, Hanseniaspora uvarum, Kluyveromyces lactis, K. marxianus, Geotrichum candidum, Pichia sp., P. guilliermondii, P. membranifaciens, Rhodotorula sp., R. mucilaginosa, Saccharomyces bayanus, S. cerevisiae, S. pastorianus, Torulaspora delbrueckii | Essential microorganisms responsible for lactic and acetic fermentation (LAB and acetic acid bacteria), alcoholic fermentation (Z. mobilis and S. cerevisase), EPS production y (Leucocnostoc sp.) and putrefactive bacteria | Lappe-Oliveras et al., 2008 |
Analysis of 16S rDNA clone libraries allowed to identify Lactobacillus acidophilus, L. kefir, L. acetotolerans, L. hilgardii, L. plantarum, Leuconostoc mesenteroides subsp. mesenteroides, L. pseudomesenteroides, Acetobacter pomorum, Gluconobacter oxydans, Zymomonas mobilis, Flavobacterium jhonsonae, Hafnia alvei | Homofermentative L. acidophilus was identified as the most abundant microorganism in three analyzed samples from different geographical origin, suggesting a possible essential role in lactic acid fermentation. L. mesenteroides was present in low proportion respect lactobacilli. Z. mobilis and AAB were detected low percentage or absent. Presence of possible putrefactive or contaminant bacteria | Escalante et al., 2004 | |
A combined culture dependent and 16S rDNA libraries approach allowed to identify those microorganisms present in freshly collected aguamiel and during a 6 h of fermentation. α-Proteobaceria: Acetobacter maloruma, A. orientalisb, Z. mobilis subsp. pomaceaeb, γ-Proteobacteria: Citrobacter sp., Enterobacter sp.a, E. agglomeransa, Erwinia rhaponticia, Kuyvera acorbatac, K. cochleaea, Providencia sp.a, Serratia grimensiia, Acinetobacter radioresistensb, Sterotrophomonas sp.a, Chryseobacterium sp. Firmicutes: Bacillus sp.a, B. licheniformisa, Lactobacillus sp.c, L. acidophilusb, L. hilgardiib, L. paracollinoidesb, L. sanfranciscensisb, Lactocoocus sp.a, L. lactisa, L. lactis susp. lactisa Leuconostoc kimchic, L. citreumc, L. gasocomitatumb, L. mesenteroidesc, L. pseudomesenteroidesc, Pediococcus urinaeequia, Streptococcus devieseia | S. cerevisiaeb | Leuconostoc citreum and L. kimchi species were identified as the most abundant LAB in aguamiel. After mixing fresh aguamiel with previously fermented pulque, L. acidophilus, L. mesenteroides were the most abundant LAB during 6 h of fermentation. E. agglomerans was the most abundant non-LAB during the first 3 h of fermentation. Z. mobilis and AAB were absent in aguamiel but detected in low proportion during the fermentation process Total bacterial counts (CFU/mL) for LAB and total aerobic mesophilic bacteria were constant during 6 h of fermentation. Total yeast counts (CFU/mL) detected in aguamiel increased after mixing aguamiel with fermented pulque, increased until 3 h and maintained constant until the end of the fermentation | Escalante et al., 2008 |
(+) Indicates killer activity detected.
Identified from a culture isolate.
Identified from 16S rDNA clone library.
Identified by culture and non-culture dependent approaches.