T 1070/00 (Antibiotic clustered genes/DSM) 23-10-2003

Main request

Articles 123(2),(3) and 84 EPC

1. Claim 1 differs from granted claim 1 in that it requires the presence of an individual regulatory region for each gene, wherein the word "individual" has been introduced into granted claim 1. This amendment restricts the claimed DNA constructs to those comprising monocistronic clustered genes and excludes genes clustered in a polycistronic manner. Thus, the requirements of Article 123(3) EPC are fulfilled.

2. The application as filed refers to general DNA fragments used for producing the claimed DNA constructs. It is stated that depending on the source of these fragments various expression cassettes may be constructed, in particular with "genomic DNA from a bacterium, the fragment containing a mono- or polycistronic coding region may include its own transcriptional initiation regulatory region ... Where genomic DNA is from fungus, normally only one gene will be associated with a transcriptional initiation regulatory region, so that each gene will have its own independent transcriptional initiation regulatory region" (page 5, lines 40 to 46). On page 4, lines 26 to 27, there is a general reference to identified DNA fragments "which include sequences which are mono- or polycistronic" without a limitation to any specific source. Thus, there is a basis for general monocistronic clusters independently of the source of the DNA fragments used. The word "individual" finds a basis in the expression "its own independent", which reflects a monocistronic organization of a gene with its (own independent, individual) regulatory region. Thus, the requirements of Article 123(2) EPC are considered to be fulfilled.

3. No objections have been raised under Article 84 EPC and the board sees none.

Article 54(3),(4) EPC

4. Document D14 discloses a BamHI DNA fragment from Streptomyces clavuligerus comprising the expandase gene responsible for the initial penicillin ring-expansion of the cephalosporin biosynthetic pathway. This 3kb BamHI DNA fragment of pBROC137 (cf Figure 2(c)) is further subcloned and screened for expandase activity (cf pBROC141, Figure 3). A fragment of pBROC141 is then used as hybridization probe for isolating an homologous DNA fragment from the Gram-negative bacteria Flavobacterium sp. SC 12,154 (cf pBROC143, Figure 1(b)), which is subcloned and screened for expandase activity too (cf pBROC148, Figure 4). By using an hybridization probe comprising the isopenicillin N synthetase (IPNS) gene from Penicillium chysogenum, pBROC143 is also shown to comprise a DNA fragment having a high degree of homology with said IPNS gene - being the IPNS enzyme responsible for the conversion of isopenicillin N to penicillin N.

5. A BamHI fragment of pBROC143 is further used as an hybridization probe for isolating cosmids pBROC155 and pBROC156 (about 35 kb), which comprise the genomic DNA from Flavobacterium occurring next to the IPNS, expandase and epimerase genes of pBROC143. By probing total chromosomal DNA from P. chysogenum with fragments of pBROC155 and, assuming that the only antibiotic genes that P. chrysogenum (penicillin- producer but not cephalosporin) has in common with Flavobacterium (cephalosporin-producer but not penicillin) are those concerned with the biosynthesis of isopenicillin N from its constituent amino acids (ie IPNS and tripeptide ACV synthetase genes), it is possible to identify two fragments of pBROC155 which comprise the gene involved in the biosynthesis of the ACV tripeptide (TPS/VE, two contiguous BamHI fragments of 3.0 and 2.2 kb) and the previously identified IPNS gene (CXI, 6.3 kb BamHI fragment) (cf Figure 1(a)).

6. Document D14 further discloses the isolation of clone pCX3.2 from a cosmid gene library of P. chrysogenum. Cosmid clone pCX3.2 has been deposited under the terms of the Budapest Treaty and comprises a 38 kb insert of genomic DNA from P. chrysogenum. By cross-hybridization studies with the TPS/VE and IPNS fragments from Flavobacterium (cf point 5 supra), pCX3.2 is shown to comprise both an ACV synthetase region and the IPNS gene (cf Figure 6(b)). The presence of ACV synthetase activity is demonstrated by showing that the transformation by pCX3.2 of an Aspergillus nidulans strain NPA5 - with a mutation that blocks the ACV synthesis - results in the production of penicillin.

7. All this information is found in the priority document D21. Figure 6(b) of document D21 identifies a 13.5 kb DNA(I) fragment of pCX3.2 comprising the ACVS region closely linked to the IPNS gene. This DNA(I) fragment, which is said to be a specific embodiment of the invention (cf page 5, second full paragraph), is characterized by its restriction map, a specific (kb) length and the presence of these ACVS and IPNS genes. Furthermore, this DNA(I) fragment is explicitly identified as carrying a "cluster" (cf page 10, second full paragraph and page 35, first paragraph). Document D21 not only discloses the deposited pCX3.2 and this DNA(I) fragment but it further shows the presence of five shorter fragments, namely pGXS10, pGXS11, pGX-C1, pGXE1 and pCYX4, wherein the two latter ones are identified as comprising, respectively, the ACVS gene (pGXE1) and the IPNS gene (pCYX4). These fragments are also characterized by their specific restriction maps, (kb) lengths and presence of the identified genes and they are made readily available to the skilled person by the deposited pCX3.2.

8. In the light of this disclosure, the board considers that the ACVS and IPNS cluster from P. chrysogenum is clearly characterized in document D14 and its priority document D21 (9 December 1987). Moreover, the ACVS and IPNS cluster is identified as a cluster in a DNA construct having all the features that define the subject-matter as claimed.

9. The respondent has argued that the presence of a DNA construct with a cluster such as the claimed one is not clearly and unambiguously derivable from document D14, in particular due to a lack of a clear and unambiguous evidence for: (i) the presence and location of the ACVS and IPNS genes, (ii) the absence of any intermediate (non-related) gene in- between the ACVS and IPNS genes and (iii) the presence of an individual regulatory region for each the ACVS and the IPNS genes. The board, however, cannot agree with the respondent's argumentation for the following reasons:

9.1. In contrast to Figures 1 to 5, wherein the (epimerase, expandase) genes identified by hybridization are not indicated as such in any restriction fragment, Figure 6 shows the clustered position of the ACVS and IPNS genes in the restriction fragments of both Flavobacterium and P. chrysogenum (cf Figures 6(a) and 6(b)). There is nothing in document D14 suggesting that the position of these genes in Figure 6 and, more particularly in the DNA(I) fragment of Figure 6(b), should be understood as being only hypothetical or provisional.

9.2. It has been argued that, whereas in Flavobacterium the ACVS gene is identified in a short, contiguous 5.5 kb BamHI fragment (cf Figure 6(a)), in P. chrysogenum this ACVS gene is spread over a longer 8 kb EcoRI fragment with three non- contiguous hybridization regions (cf Figure 6(b)) and that this difference would immediately raise doubts in the mind of the skilled person who would conclude that the position of the ACVS gene in pCX3.2 is not reliably identified. This line of argumentation, however, cannot be followed. In the light of the known differences between prokaryote and eukaryote genomes, such as the presence of introns, sequence duplications, etc. a different hybridization pattern cannot be seen as surprising but only as reflecting the normal difference between prokaryote (Flavobacterium) and eukaryote (Penicillium) genes. The complementation studies demonstrate the presence of the ACVS gene in pCX3.2, whereas the hybridization studies show that there is only one region in pCX3.2 hybridizing to an ACVS probe, namely one closely clustered to the IPNS gene. There is no reason to doubt on the presence and the position of the ACVS gene in pCX3.2 as shown in Figure 6(b).

9.3. The IPNS gene from P. chrysogenum is easily identified by its (known) restriction map in the 1.4 kb XbaI-BglII fragment of pCYX4 (cf page 260, right-hand column and Figure 2 of document D27). In a similar manner, pGXE1 comprising the ACVS region, and pGXS11 and pGXS10 comprising two contiguous DNA fragments covering said ACVS region, are also available to the skilled person (cf point 7 supra), who can, if necessary, check the information disclosed in Figure 6(b). In fact, document D14 uses the 8.0 kb EcoRI fragment from pGXE1 to obtain the plasmid vector pPEN3 which shows, as expected, elevated levels of ACVS activity in P. chrysogenum transformants (cf page 18, preparation 15 page 18). Even if pPEN13 does not enjoy priority rights - preparation 15 is not found in document D21 - it, nevertheless, confirms the characterization of the pGXE1 fragment, already present in the priority document D21 as well as pGXS11 and pGXS10. Thus, there is no reason for the skilled person to consider the information of Figure 6(b) as regards the presence and location of the ACVS and the IPNS as being doubtful or ambiguous.

9.4. In this respect too, Figure 6(b) discloses two pCX3.2 fragments covering the intermediate region along the ACVS and the IPNS genes, namely pGX-C1 and pGXS11. The board fails to find any suggestion in document D14 for the presence of an intermediate gene in-between the disclosed ACVS and IPNS genes, let alone a functionally non-related gene as defined in the patent in suit (cf page 6, lines 9 to 11 of the patent in suit). There is no intermediate gene shown in Figure 6(b) and there is no reason for the skilled person to expect one in this particular region. The board notes that even the patent in suit, without providing any further technical evidence (such as the complete nucleotide sequence of this intermediate region), explicitly acknowledges that the "ACVS gene(s) is also clustered to the (IPNS plus AT) gene cluster" (cf page 9, line 27 of the patent in suit) and thus, clustered in the manner as defined in the patent itself. No technical evidence has been put forward to contradict this. To accept that document D14 does not clearly and unambiguously disclose the absence of an intermediate non-related gene would be to apply a different standard to the disclosure of this prior art than to the patent in suit which would be contrary to the established case law (cf T 1099/99 of 4 December 2002).

9.5. Similarly, as regards the presence of an individual regulatory region for each of the ACVS and IPNS genes, the skilled person in reading document D14 has to assume, as the patent in suit has also done, that being the source genomic DNA from fungus, "normally only one gene will be associated with a transcriptional initiation regulatory region, so that each gene will have its own independent transcriptional initiation regulatory region" (cf page 5, lines 44 to 46 of the patent in suit). No technical evidence has been put forward to contradict this assumption and, as stated in point 9.4 supra, the same standard has to be apply for both the prior art and the patent in suit.

9.6. In the present case, however, the position of the 5' flanking region of the P. chrysogenum IPNS gene and its transcription initiation site are known from document D27 (cf Figure 2), as it is also rightly reflected by the presence of the IPNS transcription arrow in Figure 6(b) of document D14. The 5' flanking regions of the closely related IPNS genes from A. nidulans and C. acremonium are highly homologous and known from the prior art too (cf page 175, right-hand column, second full paragraph and Figure 4 in document D18). Thus, the assumption of an individual regulatory region for the IPNS gene is not contradicted by any prior art document on file. Moreover, the complementation studies disclosed in document D14 - as well as in the priority document D21 - demonstrate a successful transcription and translation of the ACVS gene present in pCX3.2. The fact that the IPNS translation arrow in Figure 6(b) runs in a direction opposite to the ACVS gene, implicitly indicates the presence of an individual regulatory region for the ACVS gene, even if the position of this regulatory region is not localized in Figure 6(b). This information is further supported by the elevated levels of ACVS activity found in P. chrysogenum transformants after transformation with plasmid vector pPEN3 which, as stated in point 9.3 supra, comprises the pGXE1 fragment shown in Figure 6(b) and not the 5' flanking (regulatory) region of the IPNS gene.

9.7. It has further been argued that the results of the complementation assays with pCX3.2 shown in document D14 are ambiguous as they are said to vary "from slightly less than wild type to slightly greater than the non-producing controls" (cf page 17, lines 4 to 6). However, document D14 refers to possible reasons thereof, such as decreased growth rates, inefficient expression of heterologous genes, etc. and concludes, nevertheless, that these results indicate that the gene cluster of pCX3.2 can restore the ability to produce penicillin. Reference has also been made to post-published documents as showing that fragment pGXE1 does not comprise the complete ACVS gene but only a (5' and 3') truncated ACVS gene. Thus, the presence of an elevated ACVS activity found with pPEN3 must allegedly be due to other reasons, such as an enhanced expression of endogenous ACVS gene from the transformed P. chrysogenum. This additional information is, however, not directly derivable from document D14 and, even if assuming that pGXE1 does not comprise the complete ACVS gene, this result does not rule out the presence of an individual regulatory region for the ACVS gene. In fact, this information is not considered to be relevant as the deposited pCX3.2 actually comprises all the additional 5' and 3' flanking regions of the ACVS gene - as shown in Figure 6(b) - and thus, the complete ACVS gene.

9.8. None of the prior art documents on file contradicts the technical evidence provided by document D14 and directly conveyed to the skilled person, namely the presence in the DNA construct pCX3.2 of the ACVS and IPNS genes clustered in the manner as defined in the patent in suit (cf Figure 6(b)). Moreover, there is no post-published prior art document on file demonstrating that this information directly derivable from document D14 - and its priority document D21 - is wrong or misleading.

10. Therefore, the board concludes that the claimed subject- matter does not fulfil the requirements of Article 54(3),(4) EPC.

Auxiliary request

Articles 123(2),(3) and 84 EPC

11. Apart from the objection raised under Article 123(2) EPC for the main request (cf point 2 supra), which has been maintained for this request, no further objections have been raised under Articles 123(2),(3) and 84 EPC. The board sees none and, in line with the argumentation followed for the main request, which is considered to apply to this request too, the requirements of all these Articles are considered to be fulfilled.

Article 54(3),(4) EPC

12. The teachings of document D14 are neither limited to scientific research nor to the specific ACVS gene and enzyme. Document D14 refers to the general use of "the DNA of the invention ... in many areas of industrial activity" (cf page 7, line 58), wherein the DNA according to the invention includes the deposited pCX3.2 (cf page 6, lines 16 to 24). In particular, it is explicitly stated that "recombinant vectors containing said DNA may be of value, when transformed into suitable hosts, in the production of genetically modified micro-organism which synthesize increased amounts of valuable antibiotics" (emphasis added by the board) (cf page 8, lines 2 to 6). More particularly, claim 14 comprises a method of producing penicillin from a naturally penicillin-producer host using a vector as claimed in claim 9, ie the designated pCX3.2. In the light of this disclosure, the board considers that the identification of clones producing increased or higher levels of penicillin is implicitly comprised in the method of document D14.

13. The board further notes that whereas claim 1 of this request explicitly requires the above indicated step of identifying clones producing secondary metabolite at a higher level, this step is absent in the method of claim 2 which only requires growing the transformed host comprising an extra copy of a sequence comprising a DNA construct with the clustered genes so as to have an enhanced production of antibiotic and isolating the resulting antibiotic product. Thus, such a method is clearly disclosed in document D14.

14. Thus, the board considers that the requirements of Article 54(3),(4) EPC are not met.