TABLE 2.

Primers used for PCR experiments and gene cloning and RT-PCR experiments

Gene	Positiona	Primer used for:
		PCR
luxA	A	5′ ATGCGGCATTTATTTTGGAGG 3′
	B	5′ CGGTGACCAGCACCTGC 3′
galE	A	5′ ATGCAGGTGTTGGTCACCGGCG 3′
	B	5′ CAAAGTTCATAAGCCATTCTGCCACG 3′
pgm	A	5′ ATGGCGGTATTGCAGATTG 3′
	B	5′ TCAGGTGATGACAGTGGGG 3′
galU	A	5′ ATGGCTGAAGTGCGCAAGGC 3′
	B	5′ ACCCACCACCGGACGGGC 3′
		RT-PCR
rbn	1	5′ ATGTCCCGAAAGCGATGGT 3′
luxA	2	5′ TAAATGCCGCATCCACCCCG 3′
	3	5′ ATGCGGCATTTATTTTGGAGG 3′
galE	4	5′ CGGTGACCAGCACCTGC 3′
	5	5′ ATGCAGGTGTTGGTCACCGGCG 3′
galK	6	5′ TCACAAGGCAAAGCCCTGGGTG 3′
	7	5′ ATGAACTTTGCTCATCATATTCCTGC 3′
pgm	8	5′ TGCAATACCGCCATGGCA 3′
	9	5′ ATGGCGGTATTGCAGATTG 3′
galM	10	5′ GCCAATGGTATCGAGCAGT 3′
	11	5′ GACAACGGCATGGGCTAC 3′
mgt	12	5′ CACTTCCGTGGGCTC 3′

^aPosition relative to genes shown in Fig. 1A and B.