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. 2016 Mar 7;82(6):1646–1652. doi: 10.1128/AEM.02917-15

TABLE 1.

Candidate genes involved in MZ1T flocculationa

% SNP Gene Gene product function Type of mutation Base change (NextGENe software) Amino acid change Coverage Mutant strain
100 tmz1t_3249 Polysaccharide deacetylase Nonsense G to A W111 stop 12× 20A
90 tmz1t_3637 Family 2 glycosyltransferase Frameshift G/−d V162Ab 15× 20A
93 tmz1t_3801 Polysaccharide biosynthesis CapD Nonsynonymous T to G L102Rc 29× 20A
100 tmz1t_0834 Type IV pilus assembly protein Nonsynonymous G to A A36Tb 17× 39A
100 tmz1t_1376 ABC transporter Nonsynonymous G to A G170Rc 19× 39A
70 tmz1t_1383 Von Willebrand factor Nonsynonymous G to A V162Ab 17× 39A
100 tmz1t_1679 PAS/PAC sensor containing diguanylate cyclase Nonsynonymous G to A T615Ib 14× 39A
100 tmz1t_2095 CzcA family heavy-metal efflux pump Nonsynonymous A to T V57Ec 17× 39A
90 tmz1t_3143 Diguanylate cyclase Frameshift C/−d L508Wb 11× 39A
100 tmz1t_3810 Glucose-1-phosphate thymidylyltransferase Nonsynonymous G to A R128Hb 22× 39A
a

The table shows loci with %SNP values of >75% and coverage of >10×. The percentage of the single most prevalent nonreference base in the aligned column is also shown.

b

Amino acid change predicted to result in mild property change.

c

Amino acid change predicted to result in severe property change.

d

Base deletion.